'en:hereditary arterial and articular multiple calcification syndrome'
(id=9102702 ; fe=en:hereditary arterial and articular multiple calcification syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=2686 creation date=2017-10-29 touchdate=2024-09-20 01:23:02.000)

≈ 87 relations sortantes en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 26 / 1 -> syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=syndrome | rel=r_associated | relid=0 | w=26 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 25 / 0.962 -> en:hereditary n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:hereditary | rel=r_associated | relid=0 | w=25 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:acrorenal mandibular syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:acrorenal mandibular syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:adducted thumbs and arthrogryposis syndrome christian type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:adducted thumbs and arthrogryposis syndrome christian type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:anauxetic dysplasia n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:anauxetic dysplasia | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:arterial dissection and lentiginosis syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:arterial dissection and lentiginosis syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:atherosclerosis of right iliac artery n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:atherosclerosis of right iliac artery | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:autosomal recessive spastic paraplegia type 39 n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:autosomal recessive spastic paraplegia type 39 | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:bamforth syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:bamforth syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:bestrophinopathy, autosomal recessive n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:bestrophinopathy, autosomal recessive | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:bone dysplasia azouz type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:bone dysplasia azouz type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:brachioskeletogenital syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:brachioskeletogenital syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:braddock syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:braddock syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:brain calcification rajab type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:brain calcification rajab type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cardiac anomaly and heterotaxy syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cardiomyopathy and renal anomaly syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cardiomyopathy and renal anomaly syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cervical hypertrichosis and peripheral neuropathy syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cervical hypertrichosis and peripheral neuropathy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cleidorhizomelic syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital analbuminemia n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital analbuminemia | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital cataract with ataxia and deafness syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital cataract with ataxia and deafness syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital disorder of glycosylation type 1h n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital disorder of glycosylation type 1h | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital disorder of glycosylation type 2e n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital disorder of glycosylation type 2e | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital disorder of glycosylation type id n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital disorder of glycosylation type id | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital disorder of glycosylation type ie n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital disorder of glycosylation type ie | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:congenital disorder of glycosylation, type if n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:congenital disorder of glycosylation, type if | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cooper jabs syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cooper jabs syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:craniofacial ulnar renal syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:craniofacial ulnar renal syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:cutaneous photosensitivity and lethal colitis syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:cutaneous photosensitivity and lethal colitis syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:czech dysplasia, metatarsal type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:deafness and myopia syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:deafness and myopia syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:diaphanospondylodysostosis n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:diaphanospondylodysostosis | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:dissection of splenic artery n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:dissection of splenic artery | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:dyschondrosteosis and nephritis syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:ectodermal dysplasia with blindness syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:ectodermal dysplasia with blindness syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:ehlers-danlos syndrome kyphoscoliotic and deafness type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:ehlers-danlos syndrome vascular-like type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:familial median cleft of upper and lower lip n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:familial median cleft of upper and lower lip | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:fountain syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:fountain syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:generalized peeling skin syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:generalized peeling skin syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:gracile bone dysplasia n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:hall riggs syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:hall riggs syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:heart defects limb shortening n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:heart defects limb shortening | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> 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 arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:hypomandibular faciocranial dysostosis n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:hypomandibular faciocranial dysostosis | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:insulin growth factor i deficiency n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:insulin growth factor i deficiency | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:kallman syndrome with heart disease n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:kallman syndrome with heart disease | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:late-onset junctional epidermolysis bullosa n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:late-onset junctional epidermolysis bullosa | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:lethal larsen-like syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:lethal larsen-like syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:lissencephaly type 3 familial fetal akinesia sequence syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:manouvrier syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:manouvrier syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:microcephaly albinism digital anomalies syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:microcephaly albinism digital anomalies syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:morava mehes syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:moyamoya disease with early onset achalasia n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:moyamoya disease with early onset achalasia | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:najjar syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:najjar syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:occlusion of left branch retinal artery n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:occlusion of left branch retinal artery | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:occlusion of right branch retinal artery n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:occlusion of right branch retinal artery | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:oculocutaneous albinism type 6 n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:oculocutaneous albinism type 6 | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:pelviscapular dysplasia n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:pelviscapular dysplasia | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:pili torti onychodysplasia syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:pili torti onychodysplasia syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:piussan lenaerts mathieu syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:polydactyly, preaxial ii (disorder) n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:preaxial deficiency, postaxial polydactyly and hypospadias n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:primary immunodeficiency syndrome due to p14 deficiency n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:primary immunodeficiency syndrome due to p14 deficiency | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:renal dysplasia - limb defects syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:renal dysplasia - limb defects syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:robinow-like syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:robinow-like syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:scholte syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:scholte syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:short fifth metacarpal insulin resistance syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:split-hand/foot malformation 3 n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:split-hand/foot malformation 3 | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:spondyloepiphyseal dysplasia tarda kohn type n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:spondyloepiphyseal dysplasia tarda kohn type | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:timothy syndrome type 2 n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:tubular renal disease with cardiomyopathy syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:vasculitis of mesenteric artery n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:vasculitis of mesenteric artery | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:x-linked intellectual disability with ataxia and apraxia syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:x-linked intellectual disability with ataxia and apraxia syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:yemenite deaf-blind hypopigmentation syndrome n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:yemenite deaf-blind hypopigmentation syndrome | rel=r_associated | relid=0 | w=20 en:hereditary arterial and articular multiple calcification syndrome -- r_associated #0: 20 / 0.769 -> en:zellweger-like syndrome without peroxisomal anomaly n1=en:hereditary arterial and articular multiple calcification syndrome | n2=en:zellweger-like syndrome without peroxisomal anomaly | rel=r_associated | relid=0 | w=20

≈ 86 relations entrantes en:deafness and myopia syndrome --- r_associated #0: 43 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:deafness and myopia syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=43 en:insulin growth factor i deficiency --- r_associated #0: 41 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:insulin growth factor i deficiency | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=41 en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency --- r_associated #0: 40 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=40 en:zellweger-like syndrome without peroxisomal anomaly --- r_associated #0: 40 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:zellweger-like syndrome without peroxisomal anomaly | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=40 en:morava mehes syndrome --- r_associated #0: 39 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:morava mehes syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=39 en:czech dysplasia, metatarsal type --- r_associated #0: 38 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:czech dysplasia, metatarsal type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=38 en:brain calcification rajab type --- r_associated #0: 37 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:brain calcification rajab type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=37 en:acrorenal mandibular syndrome --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:acrorenal mandibular syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:anauxetic dysplasia --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:anauxetic dysplasia | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:bamforth syndrome --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:bamforth syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:congenital disorder of glycosylation type 2e --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital disorder of glycosylation type 2e | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:ehlers-danlos syndrome kyphoscoliotic and deafness type --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:ehlers-danlos syndrome kyphoscoliotic and deafness type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:hall riggs syndrome --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:hall riggs syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:occlusion of right branch retinal artery --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:occlusion of right branch retinal artery | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:oculocutaneous albinism type 6 --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:oculocutaneous albinism type 6 | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome --- r_associated #0: 35 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=35 en:congenital disorder of glycosylation type id --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital disorder of glycosylation type id | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:cooper jabs syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cooper jabs syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:ehlers-danlos syndrome vascular-like type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:generalized peeling skin syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:generalized peeling skin syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:hypomandibular faciocranial dysostosis --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:hypomandibular faciocranial dysostosis | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:piussan lenaerts mathieu syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:piussan lenaerts mathieu syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:renal dysplasia - limb defects syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:renal dysplasia - limb defects syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:scholte syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:scholte syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:yemenite deaf-blind hypopigmentation syndrome --- r_associated #0: 34 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:yemenite deaf-blind hypopigmentation syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=34 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 32 --> 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:moyamoya disease with early onset achalasia --- r_associated #0: 32 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:moyamoya disease with early onset achalasia | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=32 en:arterial dissection and lentiginosis syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:arterial dissection and lentiginosis syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:autosomal recessive spastic paraplegia type 39 --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:autosomal recessive spastic paraplegia type 39 | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:bone dysplasia azouz type --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:bone dysplasia azouz type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:brachioskeletogenital syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:brachioskeletogenital syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:craniofacial ulnar renal syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:craniofacial ulnar renal syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:ectodermal dysplasia with blindness syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:ectodermal dysplasia with blindness syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:familial median cleft of upper and lower lip --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:familial median cleft of upper and lower lip | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:late-onset junctional epidermolysis bullosa --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:late-onset junctional epidermolysis bullosa | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:vasculitis of mesenteric artery --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:vasculitis of mesenteric artery | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:x-linked intellectual disability with ataxia and apraxia syndrome --- r_associated #0: 31 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:x-linked intellectual disability with ataxia and apraxia syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=31 en:congenital analbuminemia --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital analbuminemia | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:congenital disorder of glycosylation type 1h --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital disorder of glycosylation type 1h | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:heart defects limb shortening --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:heart defects limb shortening | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:microcephaly albinism digital anomalies syndrome --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:microcephaly albinism digital anomalies syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:najjar syndrome --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:najjar syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:pelviscapular dysplasia --- r_associated #0: 30 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:pelviscapular dysplasia | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=30 en:adducted thumbs and arthrogryposis syndrome christian type --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:adducted thumbs and arthrogryposis syndrome christian type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:bestrophinopathy, autosomal recessive --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:bestrophinopathy, autosomal recessive | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:cervical hypertrichosis and peripheral neuropathy syndrome --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cervical hypertrichosis and peripheral neuropathy syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:cleidorhizomelic syndrome --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cleidorhizomelic syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:diaphanospondylodysostosis --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:diaphanospondylodysostosis | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:dissection of splenic artery --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:dissection of splenic artery | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:timothy syndrome type 2 --- r_associated #0: 29 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:timothy syndrome type 2 | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=29 en:fountain syndrome --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:fountain syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:lissencephaly type 3 familial fetal akinesia sequence syndrome --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:lissencephaly type 3 familial fetal akinesia sequence syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:manouvrier syndrome --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:manouvrier syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:polydactyly, preaxial ii (disorder) --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:polydactyly, preaxial ii (disorder) | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:spondyloepiphyseal dysplasia tarda kohn type --- r_associated #0: 28 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:spondyloepiphyseal dysplasia tarda kohn type | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=28 en:braddock syndrome --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:braddock syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:cardiomyopathy and renal anomaly syndrome --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cardiomyopathy and renal anomaly syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:congenital disorder of glycosylation, type if --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital disorder of glycosylation, type if | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:cutaneous photosensitivity and lethal colitis syndrome --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cutaneous photosensitivity and lethal colitis syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:dyschondrosteosis and nephritis syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:gracile bone dysplasia --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:gracile bone dysplasia | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:kallman syndrome with heart disease --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:kallman syndrome with heart disease | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:pili torti onychodysplasia syndrome --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:pili torti onychodysplasia syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:split-hand/foot malformation 3 --- r_associated #0: 27 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:split-hand/foot malformation 3 | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=27 en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:atherosclerosis of right iliac artery --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:atherosclerosis of right iliac artery | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:congenital cataract with ataxia and deafness syndrome --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital cataract with ataxia and deafness syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:congenital disorder of glycosylation type ie --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:congenital disorder of glycosylation type ie | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:lethal larsen-like syndrome --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:lethal larsen-like syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:occlusion of left branch retinal artery --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:occlusion of left branch retinal artery | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:primary immunodeficiency syndrome due to p14 deficiency --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:primary immunodeficiency syndrome due to p14 deficiency | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 en:robinow-like syndrome --- r_associated #0: 26 --> en:hereditary arterial and articular multiple calcification syndrome n1=en:robinow-like syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=26 syndrome --- r_associated #0: 20 --> en:hereditary arterial and articular multiple calcification syndrome n1=syndrome | n2=en:hereditary arterial and articular multiple calcification syndrome | rel=r_associated | relid=0 | w=20