'en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome'
(id=9102913 ; fe=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=13568 creation date=2017-10-29 touchdate=2025-12-02 07:02:02.000)

≈ 631 relations sortantes en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:autosomal dominant epidermolysis bullosa simplex n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:brachymesophalangy 2 and 5 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:hereditary nonpolyposis colorectal cancer n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:noonan syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:prolonged electroretinal response suppression n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:prolonged electroretinal response suppression | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 43 / 1 -> en:spinocerebellar ataxia type 6 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=43 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:alagille syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:brachydactyly with hypertension n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly with hypertension | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:familial osteochondritis dissecans n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:retinal arteriovenous malformation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal arteriovenous malformation | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 42 / 0.977 -> en:spinocerebellar ataxia type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=42 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:acute intermittent porphyria n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:aniridia and intellectual disability syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:autosomal dominant muscular dystrophy with limb girdle distribution n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant muscular dystrophy with limb girdle distribution | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:autosomal dominant pterygium of conjunctiva n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:bosley-salih-alorainy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bosley-salih-alorainy syndrome | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:familial amyloid polyneuropathy, type v n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial amyloid polyneuropathy, type v | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:heide syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:heide syndrome | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:liddle syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:peripheral resistance to thyroid hormone n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 41 / 0.953 -> en:spinocerebellar ataxia 17 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 17 | rel=r_associated | relid=0 | w=41 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:dentatorubral-pallidoluysian atrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:ectodermal dysplasia with natal teeth, turnpenny type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:hyperpigmentation, familial progressive n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:insulin autoimmune syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:kbg syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:metaphyseal dysplasia, braun-tinschert type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:spondyloepiphyseal dysplasia, kimberley type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia, kimberley type | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 40 / 0.93 -> en:ulna metaphyseal dysplasia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=40 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:al gazali aziz salem syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:al gazali aziz salem syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:cataract glaucoma syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:familial digital arthropathy and brachydactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:odontotrichoungual-digital-palmar syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:odontotrichoungual-digital-palmar syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:shprintzen-goldberg syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:shprintzen-goldberg syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 39 / 0.907 -> en:strudwick syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=39 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:carnevale hernandez castillo syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:carnevale hernandez castillo syndrome | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:cataract microcornea syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cataract microcornea syndrome | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:coloboma of macula with type b brachydactyly n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:coloboma of macula with type b brachydactyly | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:ectopia lentis, chorioretinal dystrophy, myopia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:nicolaides baraitser syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:rombo syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:rombo syndrome | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:spondyloepiphyseal dysplasia, maroteaux type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia, maroteaux type | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 38 / 0.884 -> en:synpolydactyly n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=38 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal dominant focal dystonia dyt25 type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal dominant intermediate charcot-marie-tooth disease type e n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant intermediate charcot-marie-tooth disease type e | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:dicer1 syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:hereditary cerebral amyloid angiopathy, icelandic type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:isolated autosomal dominant hypomagnesemia glaudemans type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:isolated autosomal dominant hypomagnesemia glaudemans type | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:thrombosis of retinal vein n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:thrombosis of retinal vein | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 37 / 0.86 -> en:zunich neuroectodermal syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:zunich neuroectodermal syndrome | rel=r_associated | relid=0 | w=37 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:abruzzo erickson syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:abruzzo erickson syndrome | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:acrootoocular syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acrootoocular syndrome | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:ehlers-danlos syndrome, type i n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:familial hemiplegic migraine n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:li-fraumeni syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:microphthalmia, syndromic 4 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 4 (disorder) | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 36 / 0.837 -> en:retinal microcirculation disorder n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal microcirculation disorder | rel=r_associated | relid=0 | w=36 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:acro-dermato-ungual-lacrimal-tooth syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:acrodysostosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:acromegaloid facial appearance syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acromegaloid facial appearance syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:advanced sleep-phase syndrome, familial n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:albinism, oculocutaneous n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:albinism, oculocutaneous | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:albinotic fundus n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:angioedemas, hereditary n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:angioedemas, hereditary | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:aniridia and absent patella n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aniridia and absent patella | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:autoimmune lymphoproliferative syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant charcot-marie-tooth disease type 2a1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant charcot-marie-tooth disease type 2m n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:bannayan-riley-ruvalcaba syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bannayan-riley-ruvalcaba syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:beare-stevenson cutis gyrata syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:book syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:book syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:charcot-marie-tooth disease, axonal, type 2n n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2n | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:craniofacial conodysplasia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniofacial conodysplasia syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:craniofacial deafness hand syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:craniosynostosis, type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniosynostosis, type 2 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:currarino triad n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:currarino triad | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:dermoodontodysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dermoodontodysplasia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:diabetic retinal venous beading n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:diabetic retinal venous beading | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:familial creutzfeldt-jakob n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:grayson wilbrandt corneal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:grayson wilbrandt corneal dystrophy | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:haspeslagh fryns muelenaere syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary retinal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary retinal dystrophy | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:hyperinsulinism due to insulin receptor deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:keratitis, hereditary n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:lamellar ichthyosis, autosomal dominant form n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:limb-mammary syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:limb-mammary syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:lopes gorlin syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lopes gorlin syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:marfan syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:mowat-wilson syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:neurofibromatosis 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:neurofibromatosis 1 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:peutz-jeghers syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:pfeiffer syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pfeiffer syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:piebaldism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:polydactyly, preaxial ii (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 21 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 21 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia type 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 1 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia type 4 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:spondyloepiphyseal dysplasia macdermot type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia macdermot type | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:steinfeld syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:syndromic orbital border hypoplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:timothy syndrome type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:vascular retinopathy of left eye n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vascular retinopathy of left eye | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:vasculopathy, retinal, with cerebral leukodystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vasculopathy, retinal, with cerebral leukodystrophy | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:visceral myopathy familial external ophthalmoplegia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:visceral myopathy familial external ophthalmoplegia | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:vitelliform macular dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 35 / 0.814 -> en:vitreoretinochoroidopathy (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:acromicric dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:ameloonychohypohidrotic syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:andersen syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:ataxia telangiectasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ataxia telangiectasia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant charcot-marie-tooth disease type 2c n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant macrothrombocytopenia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant macrothrombocytopenia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:beemer ertbruggen syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:beemer ertbruggen syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:behr syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:behr syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:bethlem myopathy 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:brachydactyly, type a1 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:cardiac anomaly and heterotaxy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:cataract and cardiomyopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cataract and cardiomyopathy | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:charcot-marie-tooth disease, autosomal dominant, type 2k n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, autosomal dominant, type 2k | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:choreoathetosis/spasticity, episodic n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:congenital hereditary facial paralysis with variable hearing loss syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital hereditary facial paralysis with variable hearing loss syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:craniosynostosis, philadelphia type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniosynostosis, philadelphia type | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:crome syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:crome syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:developmental malformation, deafness, dystonia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:developmental malformation, deafness, dystonia syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:diabetic intraretinal microvascular anomalies n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:diabetic intraretinal microvascular anomalies | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:ectodermal dysplasia with blindness syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:epilepsy, myoclonic, benign adult familial, type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:fatal congenital nonlysosomal heart glycogenosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:fatal congenital nonlysosomal heart glycogenosis | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:frontotemporal dementia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:gaze palsy, familial horizontal, with progressive scoliosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:gaze palsy, familial horizontal, with progressive scoliosis | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:glaucoma and sleep apnea syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glaucoma and sleep apnea syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:glomerulopathy with fibronectin deposits 2 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glomerulopathy with fibronectin deposits 2 (disorder) | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary cystatin c amyloid angiopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary gastrogenic lactose intolerance n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary motor and sensory neuropathy type i n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hereditary vitreoretinopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary vitreoretinopathy | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hernandez fragoso syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hernandez fragoso syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:ichthyosis, cyclic, with epidermolytic hyperkeratosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:image syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:image syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:isolated hypoplasia of the right ventricle n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:isolated hypoplasia of the right ventricle | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:jervell-lange nielsen syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:jervell-lange nielsen syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:jones syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:jones syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:keratoacanthoma familial n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:keratoderma, palmoplantar, diffuse n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:keratoderma, palmoplantar, diffuse | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:microphthalmia, syndromic 5 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 5 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:nance-horan syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:nance-horan syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:oliver-mcfarlane syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:oliver-mcfarlane syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:osteosclerosis, developmental delay, craniosynostosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:osteosclerosis, developmental delay, craniosynostosis syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:pelvis-shoulder dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pelvis-shoulder dysplasia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:peters-plus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:peters-plus syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:pitt-hopkins syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:port-wine stain in rubinstein-taybi syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:port-wine stain in rubinstein-taybi syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:potassium aggravated myotonia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:reis-bucklers' corneal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:retinal artery spasm n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal artery spasm | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:retinal collateral vessels n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal collateral vessels | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:retinal vascular occlusion n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal vascular occlusion | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:schaap taylor baraitser syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:schaap taylor baraitser syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:segmentation of retinal blood vessel n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:segmentation of retinal blood vessel | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:sonoda syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:sonoda syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 10 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 29 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 31 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia 36 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spinocerebellar ataxia type 5 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:spondylo-ocular syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondylo-ocular syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:syndactyly, type iii n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:tarsal-carpal coalition syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:wt limb blood syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:wt limb blood syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 34 / 0.791 -> en:yorifuji okuno syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:yorifuji okuno syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:ablepharon-macrostomia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ablepharon-macrostomia syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:alopecia, epilepsy, pyorrhea, mental subnormality n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:alopecia, epilepsy, pyorrhea, mental subnormality | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:aplasia cutis with myopia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aplasia cutis with myopia syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:arrhythmogenic right ventricular dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:arteriosclerotic retinopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:arteriosclerotic retinopathy | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:atelosteogenesis, type 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:blepharo-cheilo-dontic syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:blepharo-cheilo-dontic syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:bork stender schmidt syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bork stender schmidt syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:bornholm eye disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bornholm eye disease | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:brachydactyly with syndactyly zhao type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly with syndactyly zhao type | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:brachymorphism-onychodysplasia-dysphalangism syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachymorphism-onychodysplasia-dysphalangism syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:brittle cornea syndrome 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brittle cornea syndrome 1 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:cap myopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cap myopathy | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease type 2d n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, type 2j n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:cleidorhizomelic syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:congenital dyserythropoietic anemia, type iii n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:dentin dyspalsia, shields type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:dermoids of cornea n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dermoids of cornea | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:dyschondrosteosis and nephritis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:dystonia 12 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:dystrophia myotonica 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:familial non-autoimmune autosomal dominant hyperthyroidism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:familial spontaneous pneumothorax n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:fechtner syndrome (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:fechtner syndrome (disorder) | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hawkinsinuria n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:heart defects limb shortening n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary arterial and articular multiple calcification syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary breast and ovarian cancer syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary myopathy with early respiratory failure n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hereditary papillary renal carcinoma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary papillary renal carcinoma | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hyperinsulinism due to uncoupling protein 2 deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hypogonadism-cataract syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypogonadism-cataract syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:hypoplastic tibia and postaxial polydactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:macular coloboma, cleft palate, hallux valgus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:macular coloboma, cleft palate, hallux valgus syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:mandibulofacial dysostosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mandibulofacial dysostosis | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:martsolf syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:martsolf syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:muscular dystrophy, oculopharyngeal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:muscular dystrophy, oculopharyngeal | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:myopathy, distal, tateyama type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:najjar syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:oculodigitoesophagoduodenal syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:oculodigitoesophagoduodenal syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:ohdo syndrome, maat-kievit-brunner type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ohdo syndrome, maat-kievit-brunner type | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:retinal telangiectasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal telangiectasia | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:siegler brewer carey syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:siegler brewer carey syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 13 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 13 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 26 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 26 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 30 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 30 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia type 7 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:syndrome, branchio-oculo-facial n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:thomas syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:thomas syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:thrombosis of retinal artery n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:thrombosis of retinal artery | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:timothy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:timothy syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:transthyretin related familial amyloid cardiomyopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:ulnar-mammary syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:uveal coloboma with cleft lip and palate and intellectual disability syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:winship viljoen leary syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:winship viljoen leary syndrome | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 32 / 0.744 -> en:x-linked retinal dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:x-linked retinal dysplasia | rel=r_associated | relid=0 | w=32 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:absence of fingerprints with congenital milia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:aicardi's syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aicardi's syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:ankylosing vertebral hyperostosis with tylosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ankylosing vertebral hyperostosis with tylosis syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant ichthyosis vulgaris n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant idiopathic familial dystonia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:benign autosomal dominant osteopetrosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:blepharoptosis, myopia, ectopia lentis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:blepharoptosis, myopia, ectopia lentis syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:branchio-oto-renal syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:branchio-oto-renal syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:cahmr syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cahmr syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:chorioretinal infarction n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chorioretinal infarction | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:congenital cataract with ataxia and deafness syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:cooper jabs syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:cutis laxa, autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:diabetic retinopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:diabetic retinopathy | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:dyskeratosis congenita, autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:dysphasia, familial developmental n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dysphasia, familial developmental | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:episodic ataxia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:foxg1 syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:frontotemporal dementia, chromosome 3-linked n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:generalized myotonia of thomsen n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:glomuvenous malformations n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary choroidal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary choroidal dystrophy | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary elliptocytosis due to alpha spectrin defect n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary multiple exostoses n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary stomatocytosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hyperinsulinism due to deficiency of glucokinase n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hyperinsulinism due to hnf4a deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:hypotrichosis simplex of scalp n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:insulin-dependent diabetes mellitus secretory diarrhea syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:intellectual disability with cataract and kyphosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:intellectual disability with cataract and kyphosis syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:keratosis palmoplantaris papulosa n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:leukokeratosis, hereditary mucosal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:leukokeratosis, hereditary mucosal | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:microcornea with glaucoma and absent frontal sinus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:microphthalmia, syndromic 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 1 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:muckle-wells syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:nemaline myopathy 3 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:neurofibromatosis, type 1-like syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:neuropathy, hereditary thermosensitive n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:norrie disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:norrie disease | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:okihiro syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:orofaciodigital syndrome 9 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:orofaciodigital syndrome 9 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:parastremmatic dwarfism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:parastremmatic dwarfism | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:parietal foramina n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:parietal foramina | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:proteus-like syndrome (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:retinal embolus n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal embolus | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:retinal microembolism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal microembolism | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:retinal vasculitis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal vasculitis | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:retinal vein disorder nos n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal vein disorder nos | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:retinal venous engorgement n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal venous engorgement | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:sellars beighton syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:short stature, pituitary and cerebellar defect and small sella turcica syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia 11 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 11 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia 20 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 20 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia 27 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 27 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia type 37 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:spondyloperipheral dysplasia short ulna n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:sting-associated vasculopathy with onset in infancy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:tmem70 related mitochondrial encephalo-cardio-myopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:tmem70 related mitochondrial encephalo-cardio-myopathy | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:vascular retinopathy of right eye n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vascular retinopathy of right eye | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:waardenburg anophthalmia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:waardenburg anophthalmia syndrome | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 31 / 0.721 -> en:whyte hemingway carpal tarsal phalangeal osteolyses n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=31 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:anophthalmia plus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:anophthalmia plus syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:apert syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:apert syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:auriculo-condylar syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant beta2-microglobulinic amyloidosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant familial woolly hair n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant mutilating keratoderma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant progressive nephropathy with hypertension n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant variant form of albumin n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:basal cell nevus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:blindness, scoliosis, arachnodactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:blindness, scoliosis, arachnodactyly syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:braddock syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:branchiogenic-deafness syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:branchiogenic-deafness syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:chromosome 3q29 deletion syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:congenital dyserythropoietic anemia type iv n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital dyserythropoietic anemia type iv | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:congenital reticular ichthyosiform erythroderma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:dmd-associated dilated cardiomyopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dmd-associated dilated cardiomyopathy | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:doughnut lesions of skull, familial n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:doughnut lesions of skull, familial | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:edict syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:edict syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:ellis yale winter syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ellis yale winter syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:encephalopathy due to sulfite oxidase deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:encephalopathy due to sulfite oxidase deficiency | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:familial alzheimer-like prion disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial alzheimer-like prion disease | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:feigenbaum bergeron richardson syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:feigenbaum bergeron richardson syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:freeman-sheldon syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:geniospasm 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:glutamate dehydrogenase 1 hyperinsulinism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glutamate dehydrogenase 1 hyperinsulinism | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary diffuse gastric adenocarcinoma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary oculoleptomeningeal amyloid angiopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary sensory autonomic neuropathy, type 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:hyaline dystrophy of bruch's membrane n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:isolated cryptophthalmos n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:isolated cryptophthalmos | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:macular dystrophy, concentric annular n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:macular dystrophy, concentric annular | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:manouvrier syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:mesomelic dwarfism reinhardt pfeiffer type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:microcephaly deafness syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:microcephaly-capillary malformation syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:microphthalmia, syndromic 3 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:multiple endocrine neoplasia type 2b n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:naxos disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:naxos disease | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:oculootoradial syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:oculootoradial syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:primary pigmented nodular adrenocortical disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:progressive heterotopic heteroplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:progressive heterotopic heteroplasia | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:pulmonary hypertension in neurofibromatosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pulmonary hypertension in neurofibromatosis | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:retinal arteriovenous dilatation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal arteriovenous dilatation | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:retinal neovascularization n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal neovascularization | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:roch leri mesosomatous lipomatosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:rudd klimek syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:rudd klimek syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 28 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:spondylometaphyseal dysplasia, algerian type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondylometaphyseal dysplasia, algerian type | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:syndactyly, type iv n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndactyly, type iv | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:ter haar syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ter haar syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:vascular sheathing of retina n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:vascular sheathing of retina | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:wnt4 mullerian aplasia and ovarian dysfunction n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 30 / 0.698 -> en:zimmerman laband syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=30 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:absent corpus callosum cataract immunodeficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:absent corpus callosum cataract immunodeficiency | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:acropectoral syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acropectoral syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:albinism, ocular n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:albinism, ocular | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:alport syndrome, autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:alport syndrome, autosomal dominant | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:anophthalmia and pulmonary hypoplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:anophthalmia and pulmonary hypoplasia | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:aplasia of lacrimal and salivary glands n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:arthrogryposis, distal, type 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant ichthyosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant oculocutaneous albinism n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:brachydactyly type a5 nail dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly type a5 nail dysplasia | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:brooke-spiegler syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:cardiac glycogen phosphorylase kinase deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cardiac glycogen phosphorylase kinase deficiency | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:char syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, axonal, type 2f n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2f | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease, axonal, type 2g n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2g | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:chromosome 22q11.2 microduplication syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:cleft palate with short stature and vertebral anomaly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cleft palate with short stature and vertebral anomaly syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:congenital sutural cataract n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital sutural cataract | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:corneal dystrophy, congenital stromal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:epiphyseal dysplasia, multiple, 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:familial aplasia of the vermis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial aplasia of the vermis | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:familial hypodontia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:glycogen storage disease type iib n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glycogen storage disease type iib | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary benign intraepithelial dyskeratosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary vascular retinopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary vascular retinopathy | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:hnsha due to triosephosphate isomerase deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:holt-oram syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:holt-oram syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:huntington disease-like 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:huntington disease-like 2 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:hyperinsulinism due to hnf1a deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:hyperuricemia, anemia, renal failure syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:johnson neuroectodermal syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:johnson neuroectodermal syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:joubert syndrome with ocular defect n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:joubert syndrome with ocular defect | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:juvenile cataract, microcornea, renal glucosuria syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:juvenile cataract, microcornea, renal glucosuria syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:knobloch syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:knobloch syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:krasnow qazi syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:krasnow qazi syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:loeys-dietz syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:lymphedema and cerebral arteriovenous anomaly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lymphedema and cerebral arteriovenous anomaly syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:mcpherson clemens syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mcpherson clemens syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:median nodule of upper lip n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:median nodule of upper lip | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:melanoma astrocytoma syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:microphthalmia, syndromic 10 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 10 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:multiple epiphyseal dysplasia type 5 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:overgrowth, macrocephaly, facial dysmorphism syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:overgrowth, macrocephaly, facial dysmorphism syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:pituitary adenoma, familial isolated (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:popliteal pterygium syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:retinal vascular changes associated with aids n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal vascular changes associated with aids | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:rouleaux formation in retinal artery n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:rouleaux formation in retinal artery | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:shprintzen omphalocele syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:small patella syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:small patella syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 18 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 18 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 25 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 25 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 8 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia type 35 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 35 | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:split-hand with congenital nystagmus, fundal changes, and cataracts n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:split-hand with congenital nystagmus, fundal changes, and cataracts | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spondylocostal dysostosis 4, autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spondyloepimetaphyseal dysplasia, missouri type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepimetaphyseal dysplasia, missouri type | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:spondyloepiphyseal dysplasia reardon type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia reardon type | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:thickened earlobe with conductive deafness syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:thickened earlobe with conductive deafness syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:trigonocephaly with broad thumb syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:trigonocephaly with broad thumb syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 29 / 0.674 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=29 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:acropectorovertebral dysplasia, f-form n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:acropectorovertebral dysplasia, f-form | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:adult onset autosomal dominant leukodystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:arterial dissection and lentiginosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant cystoid macular edema n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:behavioral variant of frontotemporal dementia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:behrens baumann dust syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:behrens baumann dust syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:blau syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:brachydactyly types b and e combined n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly types b and e combined | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:capillary malformation-arteriovenous malformation (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:cataract, congenital, cerulean type 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:choreoathetosis, hypothyroidism, and neonatal respiratory distress n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:chorioretinal atrophy, progressive bifocal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chorioretinal atrophy, progressive bifocal | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:chorioretinal vascular disorder n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chorioretinal vascular disorder | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:chromosome 17q21.31 deletion syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:congenital nephrogenic diabetes insipidus n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:corneal dystrophy, posterior amorphous n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:corneal dystrophy, posterior amorphous | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:czech dysplasia, metatarsal type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:deafness and myopia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:dominant autosomal hereditary disorder, incomplete penetrance n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:dominant beta-thalassemia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:dopa-responsive dystonia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:ehlers-danlos syndrome vascular-like type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:epithelial recurrent erosion dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:faciocardiomelic dysplasia, lethal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:faciocardiomelic dysplasia, lethal | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:familial cerebral cavernous malformation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial cerebral cavernous malformation | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:familial encephalopathy with neuroserpin inclusion bodies n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary corneal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary corneal dystrophy | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary sensory and autonomic neuropathy type 1b n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary systemic amyloidosis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hip dysplasia, beukes type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hip dysplasia, beukes type | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hunter-mcalpine craniosynostosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hunter-mcalpine craniosynostosis syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:hyperinsulinemic hypoglycemia, familial, 7 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:isolated congenital alacrima n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:isolated congenital alacrima | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:kaufman oculocerebrofacial syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:kaufman oculocerebrofacial syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:laurin-sandrow syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:mammary-digital-nail syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mammary-digital-nail syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:microcephaly microcornea syndrome seemanova type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcephaly microcornea syndrome seemanova type | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:morava mehes syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:moyamoya disease with early onset achalasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:nathalie syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:nathalie syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:neurofibromatosis 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:neurofibromatosis 2 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:neuropathy, hereditary motor and sensory, okinawa type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:optic atrophy, autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:optic atrophy, autosomal dominant | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:palmoplantar keratoderma with deafness n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:palmoplantar keratoderma with deafness | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:paraganglioma and gastric stromal sarcoma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:paraganglioma and gastric stromal sarcoma | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:pseudohypoaldosteronism, type 1, dominant form n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:pten hamartoma tumor syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pten hamartoma tumor syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:schnyder crystalline corneal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:schulman upshaw syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:schulman upshaw syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 12 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 12 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 14 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 14 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:spinocerebellar ataxia 23 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 23 | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:syndactyly, type i n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:temtamy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:temtamy syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:thiel-behnke corneal dystrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:turcot syndrome (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:turcot syndrome (disorder) | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 28 / 0.651 -> en:white platelet syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:white platelet syndrome | rel=r_associated | relid=0 | w=28 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:aase smith syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aase smith syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:alpha-fetoprotein, hereditary persistence of n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:amyloid neuropathies, familial n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:amyloid neuropathies, familial | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant polycystic kidney disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant retinitis pigmentosa n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:avascular necrosis of femur head n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:avascular necrosis of femur head | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:blepharophimosis with ptosis, syndactyly, and short stature n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:blepharophimosis with ptosis, syndactyly, and short stature | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:cardiocranial syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cardiocranial syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:cerebrooculonasal syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cerebrooculonasal syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:changes in retinal vascular appearance n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:changes in retinal vascular appearance | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:chromosome 11p11.2 deletion syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chromosome 11p11.2 deletion syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:chronic atrial and intestinal dysrhythmia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:chronic atrial and intestinal dysrhythmia | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:cole disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cole disease | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:deafness-craniofacial syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:duane anomaly, myopathy, scoliosis syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:duane anomaly, myopathy, scoliosis syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:ehlers-danlos syndrome, cardiac valvular form n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ehlers-danlos syndrome, cardiac valvular form | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:familial isolated arrhythmogenic right ventricular dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:familial partial lipodystrophy, type 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:fibular aplasia and ectrodactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:fibular aplasia and ectrodactyly syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:gemss syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:gemss syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:genitopatellar syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:gracile bone dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:growth retardation, alopecia, pseudoanodontia and optic atrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hand foot uterus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:heart-hand syndrome, slovenian type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:heart-hand syndrome, slovenian type | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary cutaneous vascular syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary cutaneous vascular syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary elliptocytosis due to abnormal protein 4.1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary elliptocytosis due to beta spectrin defect in self-association n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary optic atrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary optic atrophy | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:ischemic maculopathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:ischemic maculopathy | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:isotretinoin embryopathy like syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:isotretinoin embryopathy like syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:kallman syndrome with heart disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:late-onset retinal degeneration (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:late-onset retinal degeneration (disorder) | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:leopard syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:microphthalmia, syndromic 6 (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 6 (disorder) | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:microphthalmia, syndromic 7 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microphthalmia, syndromic 7 | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:mitochondrial neurogastrointestinal encephalomyopathy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:paroxysmal extreme pain disorder n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:phosphoserine aminotransferase deficiency n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:phosphoserine aminotransferase deficiency | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:platelet-type von willebrand disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:platelet-type von willebrand disease | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:posterior segment vascular anomalies n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:posterior segment vascular anomalies | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:preaxial deficiency, postaxial polydactyly and hypospadias n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:retinal capillary closure n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal capillary closure | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:severe x-linked intellectual disability gustavson type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:severe x-linked intellectual disability gustavson type | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:short fifth metacarpal insulin resistance syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:spinocerebellar ataxia type 32 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:stenosis of retinal artery n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:stenosis of retinal artery | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:tubular renal disease with cardiomyopathy syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 27 / 0.628 -> en:wagr syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:wagr syndrome | rel=r_associated | relid=0 | w=27 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:17q11.2 microduplication syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:amelogenesis imperfecta, type ib n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:angel shaped phalangoepiphyseal dysplasia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:angel shaped phalangoepiphyseal dysplasia | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:aphalangy and syndactyly with microcephaly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant deficiency of plasminogen n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant excess of transthyretin n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant hypophosphatemic bone disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant late onset basal ganglia degeneration n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:bilateral multiple fibroadenoma of breast n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:brachydactyly type a6 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:brachydactyly, type a2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachydactyly, type a2 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:brachyolmia type 3 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:cardiomyopathy and renal anomaly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cardiomyopathy and renal anomaly syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:cardiomyopathy dilated with woolly hair and keratoderma n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cardiomyopathy dilated with woolly hair and keratoderma | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:centronuclear myopathy 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:cerebroretinal microangiopathy with calcifications and cysts (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:congenital cataracts, facial dysmorphism, and neuropathy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:congenital cataracts, facial dysmorphism, and neuropathy | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:cryptophthalmos syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:cryptophthalmos syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:dilatation vascular retinal n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dilatation vascular retinal | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:dominant autosomal hereditary disorder, complete penetrance n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:dysplasia, saddan n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:erythrokeratodermia with ataxia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:erythrokeratodermia with ataxia | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:familial benign neonatal epilepsy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:fibrodysplasia ossificans progressiva n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:glucose transporter protein type 1 deficiency syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hemochromatosis, type 4 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hemochromatosis, type 4 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary dysplasia of blood vessel n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary dysplasia of blood vessel | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary elliptocytosis due to deficiency of protein 4.1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hyperferritinemia, hereditary, with congenital cataracts n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hyperparathyroidism-jaw tumor syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:hypoparathyroidism - autosomal dominant n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hypoparathyroidism - autosomal dominant | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:jackson-weiss syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:karandikar maria kamble syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:karandikar maria kamble syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:lowry maclean syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lowry maclean syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:lymphedema, cardiac septal defects, and characteristic facies n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:lymphedema, cardiac septal defects, and characteristic facies | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:may-hegglin anomaly n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:mesomelic dysplasia, kantaputra type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mesomelic dysplasia, kantaputra type | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:microcornea with corectopia and macular hypoplasia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:microcornea with corectopia and macular hypoplasia syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:mullerian duct and limb anomalies syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:multiple epiphyseal dysplasia beighton type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:multiple epiphyseal dysplasia beighton type | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:myopathy, distal 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:occlusion of left branch retinal artery n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:occlusion of left branch retinal artery | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:occlusion of right branch retinal artery n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:occlusion of right branch retinal artery | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:osteogenesis imperfecta, levin type n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:osteopoikilosis and dacryocystitis n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:osteopoikilosis and dacryocystitis | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:other intraretinal microvascular abnormality n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:other intraretinal microvascular abnormality | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:pseudohypoparathyroidism type 1c n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pseudohypoparathyroidism type 1c | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:reticulate acropigmentation of kitamura n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:retinal capillary dilatation n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal capillary dilatation | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:retinal vein tortuosity n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:retinal vein tortuosity | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:robinow-like syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:scalp-ear-nipple syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:scalp-ear-nipple syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:schilbach-rott syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:schilbach-rott syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:short stature with valvular heart disease and characteristic facies syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia 15 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia 15 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 19 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spinocerebellar ataxia type 19 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:split-hand-foot malformation with long bone deficiency 1 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:stapes ankylosis with broad thumb and toes (disorder) n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:stapes ankylosis with broad thumb and toes (disorder) | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:steatocystoma multiplex n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:syndactyly, type v n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:syndactyly, type v | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:upington disease n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:upington disease | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:upper limb defect with eye and ear abnormalities syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:upper limb defect with eye and ear abnormalities syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> en:wellesley carman french syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 26 / 0.605 -> syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 25 / 0.581 -> en:hereditary n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:hereditary | rel=r_associated | relid=0 | w=25 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:corneal dystrophy, subepithelial mucinous n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:disorder of eye co-occurrent and due to marfan syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:disorder of eye co-occurrent and due to marfan syndrome | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:epiphyseal dysplasia, multiple, 2 n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:pigmented paravenous chorioretinal atrophy n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:pigmented paravenous chorioretinal atrophy | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | rel=r_associated | relid=0 | w=20 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome -- r_associated #0: 20 / 0.465 -> rétinite pigmentaire paraveineuse n1=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | n2=rétinite pigmentaire paraveineuse | rel=r_associated | relid=0 | w=20

≈ 658 relations entrantes en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 43 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=43 rétinite pigmentaire paraveineuse --- r_associated #0: 43 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=rétinite pigmentaire paraveineuse | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=43 en:gracile bone dysplasia --- r_associated #0: 41 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:gracile bone dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=41 en:pigmented paravenous chorioretinal atrophy --- r_associated #0: 41 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pigmented paravenous chorioretinal atrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=41 en:heart defects limb shortening --- r_associated #0: 36 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:heart defects limb shortening | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=36 en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 35 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 35 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=35 en:disorder of eye co-occurrent and due to marfan syndrome --- r_associated #0: 35 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:disorder of eye co-occurrent and due to marfan syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=35 en:morava mehes syndrome --- r_associated #0: 35 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:morava mehes syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=35 en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 35 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=35 en:cleidorhizomelic syndrome --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cleidorhizomelic syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:deafness and myopia syndrome --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:deafness and myopia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dyschondrosteosis and nephritis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:kallman syndrome with heart disease --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:kallman syndrome with heart disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:occlusion of left branch retinal artery --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:occlusion of left branch retinal artery | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:robinow-like syndrome --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:robinow-like syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:spinocerebellar ataxia type 37 --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 37 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:timothy syndrome type 2 --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:timothy syndrome type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 34 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=34 en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 32 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ehlers-danlos syndrome vascular-like type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=32 en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 32 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=32 en:cataract glaucoma syndrome --- r_associated #0: 31 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cataract glaucoma syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=31 en:cooper jabs syndrome --- r_associated #0: 31 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cooper jabs syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=31 en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 31 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=31 en:moyamoya disease with early onset achalasia --- r_associated #0: 31 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:moyamoya disease with early onset achalasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=31 en:najjar syndrome --- r_associated #0: 31 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:najjar syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=31 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:bethlem myopathy 1 --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bethlem myopathy 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:czech dysplasia, metatarsal type --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:czech dysplasia, metatarsal type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ectodermal dysplasia with blindness syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:glaucoma and sleep apnea syndrome --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glaucoma and sleep apnea syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:occlusion of right branch retinal artery --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:occlusion of right branch retinal artery | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:spinocerebellar ataxia type 32 --- r_associated #0: 30 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 32 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=30 en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:piussan lenaerts mathieu syndrome --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:piussan lenaerts mathieu syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:polydactyly, preaxial ii (disorder) --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:polydactyly, preaxial ii (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:primary pigmented nodular adrenocortical disease --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:primary pigmented nodular adrenocortical disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 29 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=29 en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:absence of fingerprints with congenital milia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:arterial dissection and lentiginosis syndrome --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:arterial dissection and lentiginosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 28 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 27 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27 en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 27 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27 en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 27 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27 en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 27 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=27 en:17q11.2 microduplication syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:17q11.2 microduplication syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:aniridia and intellectual disability syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aniridia and intellectual disability syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:braddock syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:braddock syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:cardiomyopathy and renal anomaly syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cardiomyopathy and renal anomaly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:corneal dystrophy, subepithelial mucinous | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 en:manouvrier syndrome --- r_associated #0: 26 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:manouvrier syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=26 démence fronto-temporale --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=démence fronto-temporale | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:aase smith syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aase smith syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ablepharon-macrostomia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ablepharon-macrostomia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:abruzzo erickson syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:abruzzo erickson syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:absent corpus callosum cataract immunodeficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:absent corpus callosum cataract immunodeficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acrodysostosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acrodysostosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acromegaloid facial appearance syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acromegaloid facial appearance syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acromicric dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acromicric dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acrootoocular syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acrootoocular syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acropectoral syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acropectoral syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acropectorovertebral dysplasia, f-form --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acropectorovertebral dysplasia, f-form | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:acute intermittent porphyria --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:acute intermittent porphyria | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:adult onset autosomal dominant leukodystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:advanced sleep-phase syndrome, familial --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:advanced sleep-phase syndrome, familial | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:aicardi's syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aicardi's syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:al gazali aziz salem syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:al gazali aziz salem syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:alagille syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:alagille syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:albinism, ocular --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:albinism, ocular | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:albinism, oculocutaneous --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:albinism, oculocutaneous | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:albinotic fundus --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:albinotic fundus | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:alopecia, epilepsy, pyorrhea, mental subnormality --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:alopecia, epilepsy, pyorrhea, mental subnormality | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:alport syndrome, autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:alport syndrome, autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:amelogenesis imperfecta, type ib --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:amelogenesis imperfecta, type ib | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ameloonychohypohidrotic syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ameloonychohypohidrotic syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:amyloid neuropathies, familial --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:amyloid neuropathies, familial | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:andersen syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:andersen syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:angel shaped phalangoepiphyseal dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:angel shaped phalangoepiphyseal dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:angioedemas, hereditary --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:angioedemas, hereditary | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:aniridia and absent patella --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aniridia and absent patella | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ankylosing vertebral hyperostosis with tylosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ankylosing vertebral hyperostosis with tylosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia and pulmonary hypoplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:anophthalmia and pulmonary hypoplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:anophthalmia plus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:anophthalmia plus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:apert syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:apert syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:aplasia cutis with myopia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aplasia cutis with myopia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:aplasia of lacrimal and salivary glands --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:aplasia of lacrimal and salivary glands | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:arrhythmogenic right ventricular dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:arteriosclerotic retinopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:arteriosclerotic retinopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:arthrogryposis, distal, type 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:arthrogryposis, distal, type 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ataxia telangiectasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ataxia telangiectasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:atelosteogenesis, type 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:atelosteogenesis, type 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:auriculo-condylar syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:auriculo-condylar syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autoimmune lymphoproliferative syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autoimmune lymphoproliferative syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant cystoid macular edema --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant cystoid macular edema | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant deficiency of plasminogen --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant deficiency of plasminogen | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant epidermolysis bullosa simplex --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant epidermolysis bullosa simplex | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant excess of transthyretin --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant excess of transthyretin | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant familial woolly hair --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant familial woolly hair | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant ichthyosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant ichthyosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant ichthyosis vulgaris | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant idiopathic familial dystonia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant intermediate charcot-marie-tooth disease type e --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant intermediate charcot-marie-tooth disease type e | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant macrothrombocytopenia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant macrothrombocytopenia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant muscular dystrophy with limb girdle distribution --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant muscular dystrophy with limb girdle distribution | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant mutilating keratoderma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant mutilating keratoderma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant oculocutaneous albinism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant oculocutaneous albinism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant polycystic kidney disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant polycystic kidney disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant pterygium of conjunctiva | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant retinitis pigmentosa --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant retinitis pigmentosa | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:autosomal dominant variant form of albumin --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:autosomal dominant variant form of albumin | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:avascular necrosis of femur head --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:avascular necrosis of femur head | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bannayan-riley-ruvalcaba syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bannayan-riley-ruvalcaba syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:basal cell nevus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:basal cell nevus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:beare-stevenson cutis gyrata syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:beemer ertbruggen syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:beemer ertbruggen syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:behavioral variant of frontotemporal dementia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:behavioral variant of frontotemporal dementia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:behr syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:behr syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:behrens baumann dust syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:behrens baumann dust syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:benign autosomal dominant osteopetrosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:benign autosomal dominant osteopetrosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bilateral multiple fibroadenoma of breast --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bilateral multiple fibroadenoma of breast | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:blau syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:blau syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:blepharo-cheilo-dontic syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:blepharo-cheilo-dontic syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:blepharophimosis with ptosis, syndactyly, and short stature --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:blepharophimosis with ptosis, syndactyly, and short stature | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:blepharoptosis, myopia, ectopia lentis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:blepharoptosis, myopia, ectopia lentis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:blindness, scoliosis, arachnodactyly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:blindness, scoliosis, arachnodactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:book syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:book syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bork stender schmidt syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bork stender schmidt syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bornholm eye disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bornholm eye disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:bosley-salih-alorainy syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:bosley-salih-alorainy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly type a5 nail dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly type a5 nail dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly type a6 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly type a6 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly types b and e combined --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly types b and e combined | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly with hypertension --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly with hypertension | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly with syndactyly zhao type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly with syndactyly zhao type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a1 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly, type a1 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachydactyly, type a2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachydactyly, type a2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachymesophalangy 2 and 5 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachymesophalangy 2 and 5 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachymorphism-onychodysplasia-dysphalangism syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachymorphism-onychodysplasia-dysphalangism syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brachyolmia type 3 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brachyolmia type 3 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:branchio-oto-renal syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:branchio-oto-renal syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:branchiogenic-deafness syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:branchiogenic-deafness syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brittle cornea syndrome 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brittle cornea syndrome 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:brooke-spiegler syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:brooke-spiegler syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cahmr syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cahmr syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cap myopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cap myopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cardiac glycogen phosphorylase kinase deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cardiac glycogen phosphorylase kinase deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cardiocranial syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cardiocranial syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cardiomyopathy dilated with woolly hair and keratoderma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cardiomyopathy dilated with woolly hair and keratoderma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:carnevale hernandez castillo syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:carnevale hernandez castillo syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cataract and cardiomyopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cataract and cardiomyopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cataract microcornea syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cataract microcornea syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cataract, congenital, cerulean type 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cataract, congenital, cerulean type 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:centronuclear myopathy 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:centronuclear myopathy 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cerebrooculonasal syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cerebrooculonasal syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cerebroretinal microangiopathy with calcifications and cysts (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cerebroretinal microangiopathy with calcifications and cysts (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:changes in retinal vascular appearance --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:changes in retinal vascular appearance | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:char syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:char syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease type 2d --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease type 2d | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, autosomal dominant, type 2k --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, autosomal dominant, type 2k | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2f --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2f | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2g --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2g | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, axonal, type 2n --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, axonal, type 2n | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:charcot-marie-tooth disease, type 2j --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:charcot-marie-tooth disease, type 2j | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:choreoathetosis, hypothyroidism, and neonatal respiratory distress --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:choreoathetosis, hypothyroidism, and neonatal respiratory distress | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:choreoathetosis/spasticity, episodic --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:choreoathetosis/spasticity, episodic | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chorioretinal atrophy, progressive bifocal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chorioretinal atrophy, progressive bifocal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chorioretinal infarction --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chorioretinal infarction | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chorioretinal vascular disorder --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chorioretinal vascular disorder | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 11p11.2 deletion syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chromosome 11p11.2 deletion syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chromosome 17q21.31 deletion syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chromosome 3q29 deletion syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chromosome 3q29 deletion syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:chronic atrial and intestinal dysrhythmia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:chronic atrial and intestinal dysrhythmia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cleft palate with short stature and vertebral anomaly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cleft palate with short stature and vertebral anomaly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cleidocranial dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cleidocranial dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cole disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cole disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:coloboma of macula with type b brachydactyly --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:coloboma of macula with type b brachydactyly | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital cataracts, facial dysmorphism, and neuropathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital cataracts, facial dysmorphism, and neuropathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia type iv --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital dyserythropoietic anemia type iv | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital dyserythropoietic anemia, type iii | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital hereditary facial paralysis with variable hearing loss syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital hereditary facial paralysis with variable hearing loss syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital muscular dystrophy with infantile cataract and hypogonadism syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital nephrogenic diabetes insipidus --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital nephrogenic diabetes insipidus | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital reticular ichthyosiform erythroderma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:congenital sutural cataract --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:congenital sutural cataract | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:corneal dystrophy, congenital stromal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:corneal dystrophy, congenital stromal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:corneal dystrophy, posterior amorphous --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:corneal dystrophy, posterior amorphous | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:craniofacial conodysplasia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniofacial conodysplasia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:craniofacial deafness hand syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniofacial deafness hand syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniosynostosis with dandy-walker malformation and hydrocephalus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis, philadelphia type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniosynostosis, philadelphia type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:craniosynostosis, type 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:craniosynostosis, type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:crome syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:crome syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cryptophthalmos syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cryptophthalmos syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:currarino triad --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:currarino triad | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:cutis laxa, autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:cutis laxa, autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:deafness-craniofacial syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:deafness-craniofacial syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dentatorubral-pallidoluysian atrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dentin dyspalsia, shields type 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dentin dyspalsia, shields type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dermoids of cornea --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dermoids of cornea | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dermoodontodysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dermoodontodysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:developmental malformation, deafness, dystonia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:developmental malformation, deafness, dystonia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:diabetic intraretinal microvascular anomalies --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:diabetic intraretinal microvascular anomalies | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:diabetic retinal venous beading --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:diabetic retinal venous beading | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:diabetic retinopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:diabetic retinopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dicer1 syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dicer1 syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dilatation vascular retinal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dilatation vascular retinal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dmd-associated dilated cardiomyopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dmd-associated dilated cardiomyopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dominant beta-thalassemia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dominant beta-thalassemia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dopa-responsive dystonia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dopa-responsive dystonia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:doughnut lesions of skull, familial --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:doughnut lesions of skull, familial | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:duane anomaly, myopathy, scoliosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:duane anomaly, myopathy, scoliosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dyskeratosis congenita, autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dysphasia, familial developmental --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dysphasia, familial developmental | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dysplasia, saddan --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dysplasia, saddan | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dystonia 12 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dystonia 12 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:dystrophia myotonica 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:dystrophia myotonica 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ectopia lentis, chorioretinal dystrophy, myopia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ectopia lentis, chorioretinal dystrophy, myopia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:edict syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:edict syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, cardiac valvular form --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ehlers-danlos syndrome, cardiac valvular form | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ehlers-danlos syndrome, type i --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ehlers-danlos syndrome, type i | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ellis yale winter syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ellis yale winter syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:encephalopathy due to sulfite oxidase deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:encephalopathy due to sulfite oxidase deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:episodic ataxia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:episodic ataxia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:epithelial recurrent erosion dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:epithelial recurrent erosion dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:erythrokeratodermia with ataxia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:erythrokeratodermia with ataxia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:faciocardiomelic dysplasia, lethal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:faciocardiomelic dysplasia, lethal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial alzheimer-like prion disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial alzheimer-like prion disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial amyloid polyneuropathy, type v --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial amyloid polyneuropathy, type v | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial aplasia of the vermis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial aplasia of the vermis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial benign neonatal epilepsy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial benign neonatal epilepsy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial cerebral cavernous malformation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial cerebral cavernous malformation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial creutzfeldt-jakob --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial creutzfeldt-jakob | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial hemiplegic migraine --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial hemiplegic migraine | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial hypodontia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial hypodontia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial osteochondritis dissecans --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial osteochondritis dissecans | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial partial lipodystrophy, type 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial partial lipodystrophy, type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:familial spontaneous pneumothorax --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:familial spontaneous pneumothorax | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:fatal congenital nonlysosomal heart glycogenosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:fatal congenital nonlysosomal heart glycogenosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:fechtner syndrome (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:fechtner syndrome (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:feigenbaum bergeron richardson syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:feigenbaum bergeron richardson syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:fibrodysplasia ossificans progressiva --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:fibrodysplasia ossificans progressiva | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:fibular aplasia and ectrodactyly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:fibular aplasia and ectrodactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:foxg1 syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:foxg1 syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:freeman-sheldon syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:freeman-sheldon syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal dementia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:frontotemporal dementia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:gaze palsy, familial horizontal, with progressive scoliosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:gaze palsy, familial horizontal, with progressive scoliosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:gemss syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:gemss syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:generalized myotonia of thomsen --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:generalized myotonia of thomsen | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:geniospasm 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:geniospasm 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:genitopatellar syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:genitopatellar syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:glomerulopathy with fibronectin deposits 2 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glomerulopathy with fibronectin deposits 2 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:glomuvenous malformations --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glomuvenous malformations | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:glutamate dehydrogenase 1 hyperinsulinism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glutamate dehydrogenase 1 hyperinsulinism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:glycogen storage disease type iib --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:glycogen storage disease type iib | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:grayson wilbrandt corneal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:grayson wilbrandt corneal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:growth retardation, alopecia, pseudoanodontia and optic atrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hand foot uterus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hand foot uterus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:haspeslagh fryns muelenaere syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hawkinsinuria --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hawkinsinuria | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:heart-hand syndrome, slovenian type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:heart-hand syndrome, slovenian type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:heide syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:heide syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hemochromatosis, type 4 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hemochromatosis, type 4 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary breast and ovarian cancer syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary choroidal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary choroidal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary corneal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary corneal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary cutaneous vascular syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary cutaneous vascular syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary cystatin c amyloid angiopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary dysplasia of blood vessel --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary dysplasia of blood vessel | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to abnormal protein 4.1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to alpha spectrin defect --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to beta spectrin defect in self-association --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary elliptocytosis due to deficiency of protein 4.1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary gastrogenic lactose intolerance --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary gastrogenic lactose intolerance | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary motor and sensory neuropathy type i --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary motor and sensory neuropathy type i | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary multiple exostoses --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary multiple exostoses | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary myopathy with early respiratory failure --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary myopathy with early respiratory failure | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary nonpolyposis colorectal cancer | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary optic atrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary optic atrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary papillary renal carcinoma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary papillary renal carcinoma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary retinal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary retinal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary stomatocytosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary stomatocytosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary systemic amyloidosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary systemic amyloidosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary vascular retinopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary vascular retinopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hereditary vitreoretinopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hereditary vitreoretinopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hernandez fragoso syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hernandez fragoso syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hip dysplasia, beukes type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hip dysplasia, beukes type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:holt-oram syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:holt-oram syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hunter-mcalpine craniosynostosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hunter-mcalpine craniosynostosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:huntington disease-like 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:huntington disease-like 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyaline dystrophy of bruch's membrane --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyaline dystrophy of bruch's membrane | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hyperpigmentation, familial progressive --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hyperpigmentation, familial progressive | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypogonadism-cataract syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypogonadism-cataract syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypoparathyroidism - autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypoparathyroidism - autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypoplasia and coloboma of alar cartilage with telecanthus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:hypotrichosis simplex of scalp --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:hypotrichosis simplex of scalp | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ichthyosis, cyclic, with epidermolytic hyperkeratosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ichthyosis, cyclic, with epidermolytic hyperkeratosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:image syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:image syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:inclusion body myopathy with early-onset paget disease and frontotemporal dementia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:insulin autoimmune syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:insulin autoimmune syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:insulin-dependent diabetes mellitus secretory diarrhea syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:insulin-dependent diabetes mellitus secretory diarrhea syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:intellectual disability with cataract and kyphosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:intellectual disability with cataract and kyphosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ischemic maculopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ischemic maculopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:isolated autosomal dominant hypomagnesemia glaudemans type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:isolated autosomal dominant hypomagnesemia glaudemans type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:isolated congenital alacrima --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:isolated congenital alacrima | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:isolated cryptophthalmos --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:isolated cryptophthalmos | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:isolated hypoplasia of the right ventricle --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:isolated hypoplasia of the right ventricle | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:isotretinoin embryopathy like syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:isotretinoin embryopathy like syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:jackson-weiss syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:jackson-weiss syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:jervell-lange nielsen syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:jervell-lange nielsen syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:johnson neuroectodermal syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:johnson neuroectodermal syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:jones syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:jones syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:joubert syndrome with ocular defect --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:joubert syndrome with ocular defect | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:juvenile cataract, microcornea, renal glucosuria syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:juvenile cataract, microcornea, renal glucosuria syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:karandikar maria kamble syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:karandikar maria kamble syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:kaufman oculocerebrofacial syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:kaufman oculocerebrofacial syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:kbg syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:kbg syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:keratitis, hereditary --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:keratitis, hereditary | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:keratoacanthoma familial --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:keratoacanthoma familial | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:keratoderma, palmoplantar, diffuse --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:keratoderma, palmoplantar, diffuse | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:keratosis palmoplantaris papulosa --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:keratosis palmoplantaris papulosa | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:knobloch syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:knobloch syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:krasnow qazi syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:krasnow qazi syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:late-onset retinal degeneration (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:late-onset retinal degeneration (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:laurin-sandrow syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:laurin-sandrow syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:leopard syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:leopard syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:leukokeratosis, hereditary mucosal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:leukokeratosis, hereditary mucosal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:li-fraumeni syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:li-fraumeni syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:liddle syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:liddle syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:limb-mammary syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:limb-mammary syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lissencephaly due to tuba1a (tubulin alpha 1a) mutation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:loeys-dietz syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:loeys-dietz syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lopes gorlin syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lopes gorlin syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lowry maclean syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lowry maclean syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lymphedema and cerebral arteriovenous anomaly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lymphedema and cerebral arteriovenous anomaly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:lymphedema, cardiac septal defects, and characteristic facies --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:lymphedema, cardiac septal defects, and characteristic facies | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:macular coloboma, cleft palate, hallux valgus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:macular coloboma, cleft palate, hallux valgus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:macular dystrophy, concentric annular --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:macular dystrophy, concentric annular | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mammary-digital-nail syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mammary-digital-nail syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mandibulofacial dysostosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mandibulofacial dysostosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:marfan syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:marfan syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:martsolf syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:martsolf syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:may-hegglin anomaly --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:may-hegglin anomaly | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mcpherson clemens syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mcpherson clemens syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:median nodule of upper lip --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:median nodule of upper lip | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:melanoma astrocytoma syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:melanoma astrocytoma syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mesomelic dysplasia, kantaputra type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mesomelic dysplasia, kantaputra type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microcephaly deafness syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microcephaly deafness syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microcephaly microcornea syndrome seemanova type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microcephaly microcornea syndrome seemanova type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microcephaly-capillary malformation syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microcephaly-capillary malformation syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microcornea with corectopia and macular hypoplasia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microcornea with corectopia and macular hypoplasia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 10 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 10 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 3 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 3 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 4 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 4 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 5 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 5 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 6 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 6 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:microphthalmia, syndromic 7 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:microphthalmia, syndromic 7 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mitochondrial neurogastrointestinal encephalomyopathy syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mitochondrial neurogastrointestinal encephalomyopathy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mowat-wilson syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mowat-wilson syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:muckle-wells syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:muckle-wells syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:mullerian duct and limb anomalies syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:mullerian duct and limb anomalies syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:multiple endocrine neoplasia type 2b --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:multiple endocrine neoplasia type 2b | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:multiple epiphyseal dysplasia beighton type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:multiple epiphyseal dysplasia beighton type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:multiple epiphyseal dysplasia type 5 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:muscular dystrophy, oculopharyngeal --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:muscular dystrophy, oculopharyngeal | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:myopathy, distal 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:myopathy, distal 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:myopathy, distal, tateyama type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:myopathy, distal, tateyama type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:nance-horan syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:nance-horan syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:nathalie syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:nathalie syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:naxos disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:naxos disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:nemaline myopathy 3 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:nemaline myopathy 3 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:neurofibromatosis 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:neurofibromatosis 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:neurofibromatosis, type 1-like syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:neuropathy, hereditary thermosensitive --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:neuropathy, hereditary thermosensitive | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:nicolaides baraitser syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:nicolaides baraitser syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:noonan syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:noonan syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:norrie disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:norrie disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:oculodigitoesophagoduodenal syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:oculodigitoesophagoduodenal syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:oculootoradial syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:oculootoradial syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:odontotrichoungual-digital-palmar syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:odontotrichoungual-digital-palmar syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ohdo syndrome, maat-kievit-brunner type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ohdo syndrome, maat-kievit-brunner type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:okihiro syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:okihiro syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:oliver-mcfarlane syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:oliver-mcfarlane syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:optic atrophy, autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:optic atrophy, autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:orofaciodigital syndrome 9 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:orofaciodigital syndrome 9 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:osteogenesis imperfecta, levin type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:osteogenesis imperfecta, levin type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:osteopoikilosis and dacryocystitis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:osteopoikilosis and dacryocystitis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:osteosclerosis, developmental delay, craniosynostosis syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:osteosclerosis, developmental delay, craniosynostosis syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:other intraretinal microvascular abnormality --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:other intraretinal microvascular abnormality | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:overgrowth, macrocephaly, facial dysmorphism syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:overgrowth, macrocephaly, facial dysmorphism syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:palmoplantar keratoderma with deafness --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:palmoplantar keratoderma with deafness | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:paraganglioma and gastric stromal sarcoma --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:paraganglioma and gastric stromal sarcoma | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:parastremmatic dwarfism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:parastremmatic dwarfism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:parietal foramina --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:parietal foramina | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:paroxysmal extreme pain disorder --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:paroxysmal extreme pain disorder | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pelvis-shoulder dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pelvis-shoulder dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:peripheral resistance to thyroid hormone --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:peripheral resistance to thyroid hormone | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:peters-plus syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:peters-plus syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:peutz-jeghers syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:peutz-jeghers syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pfeiffer syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pfeiffer syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:phosphoserine aminotransferase deficiency --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:phosphoserine aminotransferase deficiency | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:piebaldism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:piebaldism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pitt-hopkins syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pitt-hopkins syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:platelet-type von willebrand disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:platelet-type von willebrand disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:popliteal pterygium syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:popliteal pterygium syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:port-wine stain in rubinstein-taybi syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:port-wine stain in rubinstein-taybi syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:posterior segment vascular anomalies --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:posterior segment vascular anomalies | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:potassium aggravated myotonia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:potassium aggravated myotonia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:progressive heterotopic heteroplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:progressive heterotopic heteroplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:prolonged electroretinal response suppression --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:prolonged electroretinal response suppression | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:proteus-like syndrome (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:proteus-like syndrome (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pseudohypoparathyroidism type 1c --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pseudohypoparathyroidism type 1c | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pten hamartoma tumor syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pten hamartoma tumor syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:pulmonary hypertension in neurofibromatosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:pulmonary hypertension in neurofibromatosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:reis-bucklers' corneal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:reis-bucklers' corneal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:reticulate acropigmentation of kitamura --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:reticulate acropigmentation of kitamura | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal arteriovenous dilatation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal arteriovenous dilatation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal arteriovenous malformation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal arteriovenous malformation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal artery spasm --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal artery spasm | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal capillary closure --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal capillary closure | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal capillary dilatation --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal capillary dilatation | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal collateral vessels --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal collateral vessels | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal embolus --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal embolus | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal microcirculation disorder --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal microcirculation disorder | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal microembolism --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal microembolism | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal neovascularization --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal neovascularization | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal telangiectasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal telangiectasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal vascular changes associated with aids --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal vascular changes associated with aids | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal vascular occlusion --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal vascular occlusion | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal vasculitis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal vasculitis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal vein disorder nos --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal vein disorder nos | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal vein tortuosity --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal vein tortuosity | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:retinal venous engorgement --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:retinal venous engorgement | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:roch leri mesosomatous lipomatosis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:roch leri mesosomatous lipomatosis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:rombo syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:rombo syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:rouleaux formation in retinal artery --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:rouleaux formation in retinal artery | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:rudd klimek syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:rudd klimek syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:scalp-ear-nipple syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:scalp-ear-nipple syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:schaap taylor baraitser syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:schaap taylor baraitser syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:schilbach-rott syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:schilbach-rott syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:schnyder crystalline corneal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:schnyder crystalline corneal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:schulman upshaw syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:schulman upshaw syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:segmentation of retinal blood vessel --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:segmentation of retinal blood vessel | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:sellars beighton syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:sellars beighton syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:sensory ataxic neuropathy, dysarthria, and ophthalmoparesis | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:severe x-linked intellectual disability gustavson type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:severe x-linked intellectual disability gustavson type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:short stature, pituitary and cerebellar defect and small sella turcica syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:short stature, pituitary and cerebellar defect and small sella turcica syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:shprintzen omphalocele syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:shprintzen omphalocele syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:shprintzen-goldberg syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:shprintzen-goldberg syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:siegler brewer carey syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:siegler brewer carey syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:small patella syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:small patella syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:sonoda syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:sonoda syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 10 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 10 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 11 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 11 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 12 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 12 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 13 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 13 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 14 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 14 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 15 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 15 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 17 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 17 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 18 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 18 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 20 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 20 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 21 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 21 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 23 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 23 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 25 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 25 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 26 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 26 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 27 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 27 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 28 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 28 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 29 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 29 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 30 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 30 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 36 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 36 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia 8 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia 8 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 19 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 19 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 2 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 2 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 35 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 35 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 4 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 4 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 5 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 5 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spinocerebellar ataxia type 7 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spinocerebellar ataxia type 7 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:split-hand with congenital nystagmus, fundal changes, and cataracts --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:split-hand with congenital nystagmus, fundal changes, and cataracts | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondylo-ocular syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondylo-ocular syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepimetaphyseal dysplasia, missouri type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepimetaphyseal dysplasia, missouri type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia macdermot type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia macdermot type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia reardon type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia reardon type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, kimberley type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia, kimberley type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia, maroteaux type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia, maroteaux type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloepiphyseal dysplasia-brachydactyly and distinctive speech | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondylometaphyseal dysplasia, algerian type --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondylometaphyseal dysplasia, algerian type | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:spondyloperipheral dysplasia short ulna --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:spondyloperipheral dysplasia short ulna | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:stapes ankylosis with broad thumb and toes (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:stapes ankylosis with broad thumb and toes (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:steatocystoma multiplex --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:steatocystoma multiplex | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:steinfeld syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:steinfeld syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:stenosis of retinal artery --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:stenosis of retinal artery | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:sting-associated vasculopathy with onset in infancy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:strudwick syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:strudwick syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type i --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndactyly, type i | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type iii --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndactyly, type iii | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type iv --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndactyly, type iv | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndactyly, type v --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndactyly, type v | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndrome, branchio-oculo-facial --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndrome, branchio-oculo-facial | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:syndromic orbital border hypoplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:syndromic orbital border hypoplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:synpolydactyly --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:synpolydactyly | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:tarsal-carpal coalition syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:tarsal-carpal coalition syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:temtamy syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:temtamy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ter haar syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ter haar syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:thickened earlobe with conductive deafness syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:thickened earlobe with conductive deafness syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:thiel-behnke corneal dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:thiel-behnke corneal dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:thomas syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:thomas syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:thrombosis of retinal artery --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:thrombosis of retinal artery | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:thrombosis of retinal vein --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:thrombosis of retinal vein | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:timothy syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:timothy syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:tmem70 related mitochondrial encephalo-cardio-myopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:tmem70 related mitochondrial encephalo-cardio-myopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:trigonocephaly with broad thumb syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:trigonocephaly with broad thumb syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:turcot syndrome (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:turcot syndrome (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ulna metaphyseal dysplasia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:ulnar-mammary syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:ulnar-mammary syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:upington disease --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:upington disease | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:upper limb defect with eye and ear abnormalities syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:upper limb defect with eye and ear abnormalities syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:uveal coloboma with cleft lip and palate and intellectual disability syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:uveal coloboma with cleft lip and palate and intellectual disability syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vascular retinopathy of left eye --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vascular retinopathy of left eye | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vascular retinopathy of right eye --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vascular retinopathy of right eye | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vascular sheathing of retina --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vascular sheathing of retina | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vasculopathy, retinal, with cerebral leukodystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vasculopathy, retinal, with cerebral leukodystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:visceral myopathy familial external ophthalmoplegia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:visceral myopathy familial external ophthalmoplegia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vitelliform macular dystrophy --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vitelliform macular dystrophy | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:vitreoretinochoroidopathy (disorder) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:waardenburg anophthalmia syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:waardenburg anophthalmia syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:wagr syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:wagr syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:wellesley carman french syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:wellesley carman french syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:white platelet syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:white platelet syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:winship viljoen leary syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:winship viljoen leary syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:wt limb blood syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:wt limb blood syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:x-linked retinal dysplasia --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:x-linked retinal dysplasia | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:yorifuji okuno syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:yorifuji okuno syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:zimmerman laband syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:zimmerman laband syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 en:zunich neuroectodermal syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=en:zunich neuroectodermal syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=20 aclasie diaphysaire --- r_associated #0: 15 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=aclasie diaphysaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=15 chondrodysplasie héréditaire déformante --- r_associated #0: 15 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=chondrodysplasie héréditaire déformante | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=15 exostose héréditaire multiple --- r_associated #0: 15 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=exostose héréditaire multiple | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=15 absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 arachnodactylie --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=arachnodactylie | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 ataxie télangiectasie --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=ataxie télangiectasie | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 chondrodysplasie déformante héréditaire --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=chondrodysplasie déformante héréditaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 dystrophie rétinienne héréditaire --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=dystrophie rétinienne héréditaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 maladie de Bessel-Hagen --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=maladie de Bessel-Hagen | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 maladie exostosante multiple --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=maladie exostosante multiple | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 maladie ostéogénique --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=maladie ostéogénique | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 piebaldisme --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=piebaldisme | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 piébaldisme --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=piébaldisme | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 rétinite pigmentaire liée à la périphérine (pro219leu) --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=rétinite pigmentaire liée à la périphérine (pro219leu) | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 steatocystoma multiplex --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=steatocystoma multiplex | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 stéatocystomes multiples --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=stéatocystomes multiples | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 syndrome de bor --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome de bor | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 syndrome des hamartomes multiples lié à PTEN --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome des hamartomes multiples lié à PTEN | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 10 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=10 dystrophie musculaire oculo-pharyngée --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=dystrophie musculaire oculo-pharyngée | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5 dystrophie musculaire oculopharyngée --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=dystrophie musculaire oculopharyngée | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5 maladie des exostoses multiples --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=maladie des exostoses multiples | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5 neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=neuropathie sensitive héréditaire dominante de type i | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5 non précisée, dystrophie rétinienne héréditaire --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=non précisée, dystrophie rétinienne héréditaire | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5 syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | rel=r_associated | relid=0 | w=5