'en:oculodental syndrome rutherfurd syndrome'
(id=6819663 ; fe=en:oculodental syndrome rutherfurd syndrome ; type=1 ; niveau=200 ; luminosité=25 ; somme entrante=16612 creation date=2017-06-25 touchdate=2025-12-24 13:47:41.000)

≈ 387 relations sortantes en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 43 / 1 -> en:genitopatellar syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:genitopatellar syndrome | rel=r_associated | relid=0 | w=43 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 43 / 1 -> en:hereditary oculoleptomeningeal amyloid angiopathy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary oculoleptomeningeal amyloid angiopathy | rel=r_associated | relid=0 | w=43 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 42 / 0.977 -> en:generalized epilepsy and paroxysmal dyskinesia syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:generalized epilepsy and paroxysmal dyskinesia syndrome | rel=r_associated | relid=0 | w=42 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 42 / 0.977 -> en:popliteal pterygium syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:popliteal pterygium syndrome | rel=r_associated | relid=0 | w=42 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 42 / 0.977 -> en:potassium aggravated myotonia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:potassium aggravated myotonia | rel=r_associated | relid=0 | w=42 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:autosomal dominant variant form of albumin n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant variant form of albumin | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:ehlers-danlos syndrome, type i n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ehlers-danlos syndrome, type i | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:familial amyloid neuropathy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial amyloid neuropathy | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:familial hypodontia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial hypodontia | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:li-fraumeni syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:li-fraumeni syndrome | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 41 / 0.953 -> en:spinocerebellar ataxia 1s n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 1s | rel=r_associated | relid=0 | w=41 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 40 / 0.93 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough n1=en:oculodental syndrome rutherfurd syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | rel=r_associated | relid=0 | w=40 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 40 / 0.93 -> en:hereditary corneal dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary corneal dystrophy | rel=r_associated | relid=0 | w=40 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 40 / 0.93 -> en:hereditary sensory autonomic neuropathy, type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary sensory autonomic neuropathy, type 1 | rel=r_associated | relid=0 | w=40 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 40 / 0.93 -> en:laurin-sandrow syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:laurin-sandrow syndrome | rel=r_associated | relid=0 | w=40 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 39 / 0.907 -> en:haspeslagh fryns muelenaere syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:haspeslagh fryns muelenaere syndrome | rel=r_associated | relid=0 | w=39 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 39 / 0.907 -> en:liddle syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:liddle syndrome | rel=r_associated | relid=0 | w=39 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 39 / 0.907 -> en:schnyder crystalline corneal dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:schnyder crystalline corneal dystrophy | rel=r_associated | relid=0 | w=39 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 38 / 0.884 -> en:aplasia of lacrimal and salivary glands n1=en:oculodental syndrome rutherfurd syndrome | n2=en:aplasia of lacrimal and salivary glands | rel=r_associated | relid=0 | w=38 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 38 / 0.884 -> en:microcephaly deafness syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:microcephaly deafness syndrome | rel=r_associated | relid=0 | w=38 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 38 / 0.884 -> en:spinocerebellar ataxia 29 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 29 | rel=r_associated | relid=0 | w=38 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 37 / 0.86 -> en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth n1=en:oculodental syndrome rutherfurd syndrome | n2=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | rel=r_associated | relid=0 | w=37 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 37 / 0.86 -> en:autosomal dominant retinitis pigmentosa n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant retinitis pigmentosa | rel=r_associated | relid=0 | w=37 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 36 / 0.837 -> en:autosomal dominant analbuminemia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant analbuminemia | rel=r_associated | relid=0 | w=36 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 36 / 0.837 -> en:autosomal dominant pterygium of conjunctiva n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant pterygium of conjunctiva | rel=r_associated | relid=0 | w=36 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 36 / 0.837 -> en:hereditary mucosal leukokeratosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary mucosal leukokeratosis | rel=r_associated | relid=0 | w=36 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 36 / 0.837 -> en:may-hegglin anomaly n1=en:oculodental syndrome rutherfurd syndrome | n2=en:may-hegglin anomaly | rel=r_associated | relid=0 | w=36 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 36 / 0.837 -> en:multiple epiphyseal dysplasia type 5 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:multiple epiphyseal dysplasia type 5 | rel=r_associated | relid=0 | w=36 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:autosomal dominant hypophosphatemic bone disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant hypophosphatemic bone disease | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:benign autosomal dominant osteopetrosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:benign autosomal dominant osteopetrosis | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:cleidocranial dysplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cleidocranial dysplasia | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:cochleosaccular degeneration of the inner ear and progressive cataracts n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cochleosaccular degeneration of the inner ear and progressive cataracts | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:cole disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cole disease | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:craniofacial deafness hand syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:craniofacial deafness hand syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:dentatorubral-pallidoluysian atrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dentatorubral-pallidoluysian atrophy | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:dicer1 syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dicer1 syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:dominant autosomal hereditary disorder, complete penetrance n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dominant autosomal hereditary disorder, complete penetrance | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:dopa-responsive dystonia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dopa-responsive dystonia | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:episodic ataxia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:episodic ataxia | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary breast and ovarian cancer syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary breast and ovarian cancer syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary multiple exostoses n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary multiple exostoses | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hereditary papillary renal cell carcinoma n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary papillary renal cell carcinoma | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hyperinsulinemic hypoglycemia, familial, 7 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 7 | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hyperparathyroidism-jaw tumor syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperparathyroidism-jaw tumor syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:hypoplastic tibia and postaxial polydactyly syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hypoplastic tibia and postaxial polydactyly syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:marfan syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:marfan syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:myopathy, distal 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:myopathy, distal 2 | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:noonan syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:noonan syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:piebaldism n1=en:oculodental syndrome rutherfurd syndrome | n2=en:piebaldism | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:potocki-shaffer syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:potocki-shaffer syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:roch leri mesosomatous lipomatosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:roch leri mesosomatous lipomatosis | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:spinocerebellar ataxia 31 (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 31 (disorder) | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:treacher collins syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:treacher collins syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 35 / 0.814 -> en:zimmerman laband syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:zimmerman laband syndrome | rel=r_associated | relid=0 | w=35 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:atelosteogenesis, type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:atelosteogenesis, type 1 | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:autosomal dominant mutilating keratoderma n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant mutilating keratoderma | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:brachydactyly type a6 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brachydactyly type a6 | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:cerebral cavernous malformation n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cerebral cavernous malformation | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:corneal dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:corneal dystrophy | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:deafness-craniofacial syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:deafness-craniofacial syndrome | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:delayed eruption of primary teeth n1=en:oculodental syndrome rutherfurd syndrome | n2=en:delayed eruption of primary teeth | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:familial hemiplegic migraine n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial hemiplegic migraine | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:familial hypercalciuric hypocalcemia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial hypercalciuric hypocalcemia | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:frontotemporal dementia, chromosome 3-linked n1=en:oculodental syndrome rutherfurd syndrome | n2=en:frontotemporal dementia, chromosome 3-linked | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:gingival hypertrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:gingival hypertrophy | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:glomuvenous malformations n1=en:oculodental syndrome rutherfurd syndrome | n2=en:glomuvenous malformations | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:hyperferritinemia, hereditary, with congenital cataracts n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperferritinemia, hereditary, with congenital cataracts | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:iris coloboma with ptosis, hypertelorism, and mental retardation n1=en:oculodental syndrome rutherfurd syndrome | n2=en:iris coloboma with ptosis, hypertelorism, and mental retardation | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:keratosis palmoplantaris papulosa n1=en:oculodental syndrome rutherfurd syndrome | n2=en:keratosis palmoplantaris papulosa | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:melnick-fraser syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:melnick-fraser syndrome | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:microphthalmia, syndromic 3 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:microphthalmia, syndromic 3 | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:muckle-wells syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:muckle-wells syndrome | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:multiple endocrine neoplasia type 2b n1=en:oculodental syndrome rutherfurd syndrome | n2=en:multiple endocrine neoplasia type 2b | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:paroxysmal extreme pain disorder n1=en:oculodental syndrome rutherfurd syndrome | n2=en:paroxysmal extreme pain disorder | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:peripheral resistance to thyroid hormone n1=en:oculodental syndrome rutherfurd syndrome | n2=en:peripheral resistance to thyroid hormone | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:syndactyly, type iii n1=en:oculodental syndrome rutherfurd syndrome | n2=en:syndactyly, type iii | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:syndrome, branchio-oculo-facial n1=en:oculodental syndrome rutherfurd syndrome | n2=en:syndrome, branchio-oculo-facial | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:ulnar-mammary syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ulnar-mammary syndrome | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 34 / 0.791 -> en:vitreoretinochoroidopathy (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:vitreoretinochoroidopathy (disorder) | rel=r_associated | relid=0 | w=34 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:alpha-fetoprotein, hereditary persistence of n1=en:oculodental syndrome rutherfurd syndrome | n2=en:alpha-fetoprotein, hereditary persistence of | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps n1=en:oculodental syndrome rutherfurd syndrome | n2=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant charcot-marie-tooth disease type 2c n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2c | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:autosomal dominant optic atrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant optic atrophy | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:behavioral variant of frontotemporal dementia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:behavioral variant of frontotemporal dementia | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:bilateral multiple fibroadenoma of breast n1=en:oculodental syndrome rutherfurd syndrome | n2=en:bilateral multiple fibroadenoma of breast | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:charcot-marie-tooth disease, axonal, type 2e (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:chromosome 3q29 deletion syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:chromosome 3q29 deletion syndrome | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:congenital nephrogenic diabetes insipidus n1=en:oculodental syndrome rutherfurd syndrome | n2=en:congenital nephrogenic diabetes insipidus | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:crouzon syndrome with acanthosis nigricans (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:crouzon syndrome with acanthosis nigricans (disorder) | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:epiphyseal dysplasia, multiple, 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:epiphyseal dysplasia, multiple, 1 | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:familial encephalopathy with neuroserpin inclusion bodies n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial encephalopathy with neuroserpin inclusion bodies | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:feingold syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:feingold syndrome | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies n1=en:oculodental syndrome rutherfurd syndrome | n2=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:leopard syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:leopard syndrome | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:reticulate acropigmentation of kitamura n1=en:oculodental syndrome rutherfurd syndrome | n2=en:reticulate acropigmentation of kitamura | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:spinocerebellar ataxia 28 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 28 | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:steinfeld syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:steinfeld syndrome | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:sting-associated vasculopathy with onset in infancy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:sting-associated vasculopathy with onset in infancy | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:transthyretin related familial amyloid cardiomyopathy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:transthyretin related familial amyloid cardiomyopathy | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:turcot syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:turcot syndrome | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:tylosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:tylosis | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 32 / 0.744 -> en:von willebrand disease, platelet type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:von willebrand disease, platelet type | rel=r_associated | relid=0 | w=32 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:acute intermittent porphyria n1=en:oculodental syndrome rutherfurd syndrome | n2=en:acute intermittent porphyria | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:advanced sleep-phase syndrome, familial n1=en:oculodental syndrome rutherfurd syndrome | n2=en:advanced sleep-phase syndrome, familial | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:ameloonychohypohidrotic syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ameloonychohypohidrotic syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant epidermolysis bullosa simplex n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant epidermolysis bullosa simplex | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant hyperinsulinism due to sur1 deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant hyperinsulinism due to sur1 deficiency | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant idiopathic familial dystonia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant idiopathic familial dystonia | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:autosomal dominant inheritance n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant inheritance | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:brachydactyly, type a1 (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brachydactyly, type a1 (disorder) | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, axonal, type 2b (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:charcot-marie-tooth disease, type 2j n1=en:oculodental syndrome rutherfurd syndrome | n2=en:charcot-marie-tooth disease, type 2j | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:dentin dyspalsia, shields type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dentin dyspalsia, shields type 2 | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:dominant autosomal hereditary disorder, incomplete penetrance n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dominant autosomal hereditary disorder, incomplete penetrance | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:dyskeratosis congenita, autosomal dominant n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dyskeratosis congenita, autosomal dominant | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hand foot uterus syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hand foot uterus syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary benign intraepithelial dyskeratosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary benign intraepithelial dyskeratosis | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary cerebral amyloid angiopathy, icelandic type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary cerebral amyloid angiopathy, icelandic type | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary cystatin c amyloid angiopathy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary cystatin c amyloid angiopathy | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hereditary systemic amyloidosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary systemic amyloidosis | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:heritable pulmonary arterial hypertension due to bmpr2 mutation n1=en:oculodental syndrome rutherfurd syndrome | n2=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hnsha due to triosephosphate isomerase deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hnsha due to triosephosphate isomerase deficiency | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:hyperpigmentation, familial progressive n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperpigmentation, familial progressive | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:jackson-weiss syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:jackson-weiss syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:melanoma astrocytoma syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:melanoma astrocytoma syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:mesomelic dwarfism reinhardt pfeiffer type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:mesomelic dwarfism reinhardt pfeiffer type | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:metaphyseal dysplasia, braun-tinschert type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:metaphyseal dysplasia, braun-tinschert type | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:short stature with valvular heart disease and characteristic facies syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:short stature with valvular heart disease and characteristic facies syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:spinocerebellar ataxia 36 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 36 | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:type i acrocephalosyndactyly n1=en:oculodental syndrome rutherfurd syndrome | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:type v acrocephalosyndactyly n1=en:oculodental syndrome rutherfurd syndrome | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 31 / 0.721 -> en:wellesley carman french syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:wellesley carman french syndrome | rel=r_associated | relid=0 | w=31 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:arthrogryposis, distal, type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:arthrogryposis, distal, type 1 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:auriculo-condylar syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:auriculo-condylar syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant deficiency of plasminogen n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant deficiency of plasminogen | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:autosomal dominant familial woolly hair n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant familial woolly hair | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:cataract, congenital, cerulean type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:congenital reticular ichthyosiform erythroderma n1=en:oculodental syndrome rutherfurd syndrome | n2=en:congenital reticular ichthyosiform erythroderma | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:corneal dystrophy, congenital stromal n1=en:oculodental syndrome rutherfurd syndrome | n2=en:corneal dystrophy, congenital stromal | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:currarino triad n1=en:oculodental syndrome rutherfurd syndrome | n2=en:currarino triad | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:familial digital arthropathy and brachydactyly syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial digital arthropathy and brachydactyly syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:fibrodysplasia ossificans progressiva n1=en:oculodental syndrome rutherfurd syndrome | n2=en:fibrodysplasia ossificans progressiva | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:geniospasm 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:geniospasm 1 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:glucose transporter protein type 1 deficiency syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:glucose transporter protein type 1 deficiency syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:hereditary gastrogenic lactose intolerance n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary gastrogenic lactose intolerance | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:hyperinsulinemic hypoglycemia, familial, 6 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinemic hypoglycemia, familial, 6 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:kbg syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:kbg syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:lynch syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:lynch syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:parietal foramina n1=en:oculodental syndrome rutherfurd syndrome | n2=en:parietal foramina | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:proteus-like syndrome (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:proteus-like syndrome (disorder) | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:shprintzen omphalocele syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:shprintzen omphalocele syndrome | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia 8 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 8 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 2 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia type 4 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 4 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:spinocerebellar ataxia type 5 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 5 | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:syndactyly, type i n1=en:oculodental syndrome rutherfurd syndrome | n2=en:syndactyly, type i | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:synpolydactyly n1=en:oculodental syndrome rutherfurd syndrome | n2=en:synpolydactyly | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:vitelliform macular dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:vitelliform macular dystrophy | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> en:wnt4 mullerian aplasia and ovarian dysfunction n1=en:oculodental syndrome rutherfurd syndrome | n2=en:wnt4 mullerian aplasia and ovarian dysfunction | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 30 / 0.698 -> syndrome de Marfan n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de Marfan | rel=r_associated | relid=0 | w=30 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:acromicric dysplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:acromicric dysplasia | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:andersen syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:andersen syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant charcot-marie-tooth disease type 2a1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2a1 | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant late onset basal ganglia degeneration n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant late onset basal ganglia degeneration | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant oculocutaneous albinism n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant oculocutaneous albinism | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:autosomal dominant progressive nephropathy with hypertension n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant progressive nephropathy with hypertension | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:bannayan syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:bannayan syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:blau syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:blau syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:brachymesophalangy 2 and 5 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brachymesophalangy 2 and 5 | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:cap myopathy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cap myopathy | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:charcot-marie-tooth disease type 2d n1=en:oculodental syndrome rutherfurd syndrome | n2=en:charcot-marie-tooth disease type 2d | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:cutis laxa, autosomal dominant n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cutis laxa, autosomal dominant | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:ectodermal dysplasia with natal teeth, turnpenny type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ectodermal dysplasia with natal teeth, turnpenny type | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:epilepsy, myoclonic, benign adult familial, type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:epilepsy, myoclonic, benign adult familial, type 2 | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:epithelial recurrent erosion dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:epithelial recurrent erosion dystrophy | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:familial spontaneous pneumothorax n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial spontaneous pneumothorax | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:frontotemporal dementia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:frontotemporal dementia | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:hereditary elliptocytosis due to beta spectrin defect in self-association n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary elliptocytosis due to beta spectrin defect in self-association | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:keratoacanthoma familial n1=en:oculodental syndrome rutherfurd syndrome | n2=en:keratoacanthoma familial | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:lamellar ichthyosis, autosomal dominant form n1=en:oculodental syndrome rutherfurd syndrome | n2=en:lamellar ichthyosis, autosomal dominant form | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:mowat-wilson syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:mowat-wilson syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:mullerian duct and limb anomalies syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:mullerian duct and limb anomalies syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:neuropathy, hereditary thermosensitive n1=en:oculodental syndrome rutherfurd syndrome | n2=en:neuropathy, hereditary thermosensitive | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:okihiro syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:okihiro syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:pitt-hopkins syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:pitt-hopkins syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:sebastian syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:sebastian syndrome | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:spinocerebellar ataxia 10 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia 10 | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:split-hand-foot malformation with long bone deficiency 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:split-hand-foot malformation with long bone deficiency 1 | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 29 / 0.674 -> en:thiel-behnke corneal dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:thiel-behnke corneal dystrophy | rel=r_associated | relid=0 | w=29 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:adult onset autosomal dominant leukodystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:adult onset autosomal dominant leukodystrophy | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:amelogenesis imperfecta, type ib n1=en:oculodental syndrome rutherfurd syndrome | n2=en:amelogenesis imperfecta, type ib | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant cystoid macular edema n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant cystoid macular edema | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:autosomal dominant ichthyosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant ichthyosis | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:avascular necrosis of femoral head n1=en:oculodental syndrome rutherfurd syndrome | n2=en:avascular necrosis of femoral head | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:brooke-spiegler syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brooke-spiegler syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:char syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:char syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:charcot-marie-tooth disease, axonal, type 2l (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:choreoathetosis/spasticity, episodic n1=en:oculodental syndrome rutherfurd syndrome | n2=en:choreoathetosis/spasticity, episodic | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:chromosome 17q21.31 deletion syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:chromosome 17q21.31 deletion syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:dominant beta-thalassemia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dominant beta-thalassemia | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:foxg1 syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:foxg1 syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:freeman-sheldon syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:freeman-sheldon syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:goniodysgenesis-mental retardation-short stature syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:goniodysgenesis-mental retardation-short stature syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hawkinsinuria n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hawkinsinuria | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary diffuse gastric adenocarcinoma n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary diffuse gastric adenocarcinoma | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary elliptocytosis due to abnormal protein 4.1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary elliptocytosis due to abnormal protein 4.1 | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary elliptocytosis due to alpha spectrin defect n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary elliptocytosis due to alpha spectrin defect | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hereditary stomatocytosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary stomatocytosis | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:hyperinsulinism due to hnf4a deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to hnf4a deficiency | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:insulin autoimmune syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:insulin autoimmune syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:keratitis, hereditary n1=en:oculodental syndrome rutherfurd syndrome | n2=en:keratitis, hereditary | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:myopathy, distal, tateyama type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:myopathy, distal, tateyama type | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:neurofibromatosis, type 1-like syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:neurofibromatosis, type 1-like syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:osteogenesis imperfecta, levin type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:osteogenesis imperfecta, levin type | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:reis-bucklers' corneal dystrophy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:reis-bucklers' corneal dystrophy | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:sellars beighton syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:sellars beighton syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> en:steatocystoma multiplex n1=en:oculodental syndrome rutherfurd syndrome | n2=en:steatocystoma multiplex | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 28 / 0.651 -> syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome | rel=r_associated | relid=0 | w=28 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant excess of transthyretin n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant excess of transthyretin | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:autosomal dominant polycystic kidney disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant polycystic kidney disease | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:centronuclear myopathy 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:centronuclear myopathy 1 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:corneal haze n1=en:oculodental syndrome rutherfurd syndrome | n2=en:corneal haze | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:dysplasia, saddan n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dysplasia, saddan | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:dystrophia myotonica 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dystrophia myotonica 2 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:familial osteochondritis dissecans n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial osteochondritis dissecans | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:familial partial lipodystrophy, type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial partial lipodystrophy, type 2 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary angioedema n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary angioedema | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:hereditary myopathy with early respiratory failure n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary myopathy with early respiratory failure | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:hypotrichosis simplex of scalp n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hypotrichosis simplex of scalp | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:microcornea with glaucoma and absent frontal sinus syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:microcornea with glaucoma and absent frontal sinus syndrome | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:neurofibromatosis type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:neurofibromatosis type 1 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:neurofibromatosis type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:neurofibromatosis type 2 | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:neuropathy, hereditary motor and sensory, okinawa type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:neuropathy, hereditary motor and sensory, okinawa type | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:peutz-jeghers syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:polydactyly, preaxial ii (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:polydactyly, preaxial ii (disorder) | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:radial hypoplasia, triphalangeal thumbs and hypospadias n1=en:oculodental syndrome rutherfurd syndrome | n2=en:radial hypoplasia, triphalangeal thumbs and hypospadias | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:spondylocostal dysostosis 4, autosomal dominant n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spondylocostal dysostosis 4, autosomal dominant | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:spondyloperipheral dysplasia short ulna n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spondyloperipheral dysplasia short ulna | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:strudwick syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:strudwick syndrome | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:tarsal-carpal coalition syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:tarsal-carpal coalition syndrome | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 27 / 0.628 -> en:whyte hemingway carpal tarsal phalangeal osteolyses n1=en:oculodental syndrome rutherfurd syndrome | n2=en:whyte hemingway carpal tarsal phalangeal osteolyses | rel=r_associated | relid=0 | w=27 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:acrodysostosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:acrodysostosis | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:alagille syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:alagille syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:autoimmune lymphoproliferative syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autoimmune lymphoproliferative syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant hyperinsulinism due to kir6.2 deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant ichthyosis vulgaris n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant ichthyosis vulgaris | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:autosomal dominant muscular dystrophy not predominantly limb girdle n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant muscular dystrophy not predominantly limb girdle | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:beare-stevenson cutis gyrata syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:beare-stevenson cutis gyrata syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:bilateral pheochromocytoma and islet cell adenoma of the pancreas n1=en:oculodental syndrome rutherfurd syndrome | n2=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:brachyolmia type 3 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brachyolmia type 3 | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:capillary malformation-arteriovenous malformation (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:capillary malformation-arteriovenous malformation (disorder) | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:cerebral hemorrhage with amyloidosis, hereditary, dutch type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:chromosome 22q11.2 microduplication syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:chromosome 22q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:congenital dyserythropoietic anemia, type iii n1=en:oculodental syndrome rutherfurd syndrome | n2=en:congenital dyserythropoietic anemia, type iii | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:dystonia 12 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dystonia 12 | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:failure of secondary teeth eruption n1=en:oculodental syndrome rutherfurd syndrome | n2=en:failure of secondary teeth eruption | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:familial benign neonatal epilepsy n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial benign neonatal epilepsy | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:familial creutzfeldt-jakob n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial creutzfeldt-jakob | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:familial isolated arrhythmogenic right ventricular dysplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial isolated arrhythmogenic right ventricular dysplasia | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:familial non-autoimmune autosomal dominant hyperthyroidism n1=en:oculodental syndrome rutherfurd syndrome | n2=en:familial non-autoimmune autosomal dominant hyperthyroidism | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related n1=en:oculodental syndrome rutherfurd syndrome | n2=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:generalized myotonia of thomsen n1=en:oculodental syndrome rutherfurd syndrome | n2=en:generalized myotonia of thomsen | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary elliptocytosis due to deficiency of protein 4.1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary elliptocytosis due to deficiency of protein 4.1 | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary motor and sensory neuropathy type i n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary motor and sensory neuropathy type i | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:hereditary nonpolyposis colorectal cancer n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary nonpolyposis colorectal cancer | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:hyaline dystrophy of bruch's membrane n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyaline dystrophy of bruch's membrane | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:hyperinsulinism due to deficiency of glucokinase n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to deficiency of glucokinase | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:loeys-dietz syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:loeys-dietz syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:nemaline myopathy 3 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:nemaline myopathy 3 | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:nevoid basal cell carcinoma syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:nevoid basal cell carcinoma syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:nicolaides baraitser syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:nicolaides baraitser syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:pituitary adenoma, familial isolated (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:pituitary adenoma, familial isolated (disorder) | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:pseudohypoaldosteronism, type 1, dominant form n1=en:oculodental syndrome rutherfurd syndrome | n2=en:pseudohypoaldosteronism, type 1, dominant form | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 6 (disorder) n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 6 (disorder) | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:spinocerebellar ataxia type 7 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 7 | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:syndromic orbital border hypoplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:syndromic orbital border hypoplasia | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 26 / 0.605 -> en:ulna metaphyseal dysplasia syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ulna metaphyseal dysplasia syndrome | rel=r_associated | relid=0 | w=26 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 21 / 0.488 -> maladie de Marfan n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie de Marfan | rel=r_associated | relid=0 | w=21 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> aclasie diaphysaire n1=en:oculodental syndrome rutherfurd syndrome | n2=aclasie diaphysaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> arachnodactylie n1=en:oculodental syndrome rutherfurd syndrome | n2=arachnodactylie | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> cancer colo-rectal héréditaire sans polypose n1=en:oculodental syndrome rutherfurd syndrome | n2=cancer colo-rectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> cancer colorectal héréditaire sans polypose n1=en:oculodental syndrome rutherfurd syndrome | n2=cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> Cancer colorectal héréditaire sans polypose n1=en:oculodental syndrome rutherfurd syndrome | n2=Cancer colorectal héréditaire sans polypose | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> chondrodysplasie déformante héréditaire n1=en:oculodental syndrome rutherfurd syndrome | n2=chondrodysplasie déformante héréditaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> chondrodysplasie héréditaire déformante n1=en:oculodental syndrome rutherfurd syndrome | n2=chondrodysplasie héréditaire déformante | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> démence fronto-temporale n1=en:oculodental syndrome rutherfurd syndrome | n2=démence fronto-temporale | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> démence frontotemporale n1=en:oculodental syndrome rutherfurd syndrome | n2=démence frontotemporale | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> dysplasie acromicrique n1=en:oculodental syndrome rutherfurd syndrome | n2=dysplasie acromicrique | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléido-crânienne n1=en:oculodental syndrome rutherfurd syndrome | n2=dysplasie cléido-crânienne | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> dysplasie cléidocrânienne n1=en:oculodental syndrome rutherfurd syndrome | n2=dysplasie cléidocrânienne | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> dystonie dopasensible n1=en:oculodental syndrome rutherfurd syndrome | n2=dystonie dopasensible | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:17q11.2 microduplication syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:17q11.2 microduplication syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:absence of fingerprints with congenital milia syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:absence of fingerprints with congenital milia syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:acro-dermato-ungual-lacrimal-tooth syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:acro-dermato-ungual-lacrimal-tooth syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Alagille's syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Alagille's syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:aniridia and intellectual disability syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:aniridia and intellectual disability syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:aniridia, ptosis, intellectual disability, familial obesity syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges n1=en:oculodental syndrome rutherfurd syndrome | n2=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:aphalangy and syndactyly with microcephaly syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:aphalangy and syndactyly with microcephaly syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:arachnodactyly n1=en:oculodental syndrome rutherfurd syndrome | n2=en:arachnodactyly | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant beta2-microglobulinic amyloidosis n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant beta2-microglobulinic amyloidosis | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant charcot-marie-tooth disease type 2m n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant charcot-marie-tooth disease type 2m | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant focal dystonia dyt25 type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant focal dystonia dyt25 type | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:autosomal dominant palmoplantar keratoderma and congenital alopecia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:basal cell nævus n1=en:oculodental syndrome rutherfurd syndrome | n2=en:basal cell nævus | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:basal cell nevus syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:basal cell nevus syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Bessel-Hagen's disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Bessel-Hagen's disease | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:bethlem myopathy 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:bethlem myopathy 1 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:brachytelephalangy, facial dysmorphism, kallmann syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:cardiac anomaly and heterotaxy syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cardiac anomaly and heterotaxy syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:cataract glaucoma syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cataract glaucoma syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:cleidorhizomelic syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:cleidorhizomelic syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:corneal dystrophy, subepithelial mucinous n1=en:oculodental syndrome rutherfurd syndrome | n2=en:corneal dystrophy, subepithelial mucinous | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:craniosynostosis with facial dysmorphism and brachydactyly syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:czech dysplasia, metatarsal type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:czech dysplasia, metatarsal type | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:diffuse palmoplantar keratoderma and acrocyanosis syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:dyschondrosteosis and nephritis syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:dyschondrosteosis and nephritis syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:ehlers-danlos syndrome vascular-like type n1=en:oculodental syndrome rutherfurd syndrome | n2=en:ehlers-danlos syndrome vascular-like type | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:epiphyseal dysplasia, multiple, 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:epiphyseal dysplasia, multiple, 2 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Feingold syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Feingold syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:gracile bone dysplasia n1=en:oculodental syndrome rutherfurd syndrome | n2=en:gracile bone dysplasia | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> 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:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hereditary non polyposis colorectal cancer n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary non polyposis colorectal cancer | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hereditary sensory and autonomic neuropathy type 1b n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hereditary sensory and autonomic neuropathy type 1b | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to hnf1a deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to hnf1a deficiency | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to insulin receptor deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to insulin receptor deficiency | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hyperinsulinism due to uncoupling protein 2 deficiency n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperinsulinism due to uncoupling protein 2 deficiency | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:hyperuricemia, anemia, renal failure syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:hyperuricemia, anemia, renal failure syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Lynch syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Lynch syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Lynch'syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Lynch'syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Marfan's disease | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:marfan's syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:marfan's syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Marfan's syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Marfan's syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:morava mehes syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:morava mehes syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:multiple osteogenic exostoses n1=en:oculodental syndrome rutherfurd syndrome | n2=en:multiple osteogenic exostoses | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:Pitt-Hopkins syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:Pitt-Hopkins syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:piussan lenaerts mathieu syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:piussan lenaerts mathieu syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:preaxial deficiency, postaxial polydactyly and hypospadias n1=en:oculodental syndrome rutherfurd syndrome | n2=en:preaxial deficiency, postaxial polydactyly and hypospadias | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:primary pigmented nodular adrenocortical disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:primary pigmented nodular adrenocortical disease | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:short fifth metacarpal insulin resistance syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:short fifth metacarpal insulin resistance syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:spinocerebellar ataxia type 32 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 32 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:spinocerebellar ataxia type 37 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:spinocerebellar ataxia type 37 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:timothy syndrome type 2 n1=en:oculodental syndrome rutherfurd syndrome | n2=en:timothy syndrome type 2 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:tubular renal disease with cardiomyopathy syndrome n1=en:oculodental syndrome rutherfurd syndrome | n2=en:tubular renal disease with cardiomyopathy syndrome | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> en:von Recklinghausen's disease n1=en:oculodental syndrome rutherfurd syndrome | n2=en:von Recklinghausen's disease | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> exostosante (maladie) n1=en:oculodental syndrome rutherfurd syndrome | n2=exostosante (maladie) | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> exostose héréditaire multiple n1=en:oculodental syndrome rutherfurd syndrome | n2=exostose héréditaire multiple | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> goniodysgénésie-retard mental-petite taille (syndrome) n1=en:oculodental syndrome rutherfurd syndrome | n2=goniodysgénésie-retard mental-petite taille (syndrome) | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> Lynch (syndrome de) n1=en:oculodental syndrome rutherfurd syndrome | n2=Lynch (syndrome de) | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie clinique de recklinghausen n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie clinique de recklinghausen | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie de Bessel-Hagen n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie de Bessel-Hagen | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie de marfan n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie de marfan | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie de Recklinghausen n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie de Recklinghausen | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie de von Recklinghausen n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie de von Recklinghausen | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie des exostoses multiples n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie des exostoses multiples | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie exostosante multiple n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie exostosante multiple | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> maladie ostéogénique n1=en:oculodental syndrome rutherfurd syndrome | n2=maladie ostéogénique | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> Marfan (maladie de) n1=en:oculodental syndrome rutherfurd syndrome | n2=Marfan (maladie de) | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> migraine hémiplégique familiale n1=en:oculodental syndrome rutherfurd syndrome | n2=migraine hémiplégique familiale | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> naevomatose baso-cellulaire n1=en:oculodental syndrome rutherfurd syndrome | n2=naevomatose baso-cellulaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> naevomatose basocellulaire n1=en:oculodental syndrome rutherfurd syndrome | n2=naevomatose basocellulaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> nævomatose basocellulaire multiple n1=en:oculodental syndrome rutherfurd syndrome | n2=nævomatose basocellulaire multiple | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> neurofibromatose de type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=neurofibromatose de type 1 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> neuropathie héréditaire sensitive et autonome de type 1 n1=en:oculodental syndrome rutherfurd syndrome | n2=neuropathie héréditaire sensitive et autonome de type 1 | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> neuropathie héréditaire sensitive et autonome de type i n1=en:oculodental syndrome rutherfurd syndrome | n2=neuropathie héréditaire sensitive et autonome de type i | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> neuropathie sensitive héréditaire dominante de type i n1=en:oculodental syndrome rutherfurd syndrome | n2=neuropathie sensitive héréditaire dominante de type i | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> neuropathie sensitive héréditaire dominante de type I n1=en:oculodental syndrome rutherfurd syndrome | n2=neuropathie sensitive héréditaire dominante de type I | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> piébaldisme n1=en:oculodental syndrome rutherfurd syndrome | n2=piébaldisme | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> piebaldisme n1=en:oculodental syndrome rutherfurd syndrome | n2=piebaldisme | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> stomatocytose héréditaire n1=en:oculodental syndrome rutherfurd syndrome | n2=stomatocytose héréditaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'Alagille n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome d'Alagille | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome d'alagille n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome d'alagille | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome de douleur extrême paroxystique n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de douleur extrême paroxystique | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Gorlin n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de Gorlin | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome de Lynch n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de Lynch | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome de marfan n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de marfan | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome héréditaire de cancer du sein et de l'ovaire n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome héréditaire de cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire n1=en:oculodental syndrome rutherfurd syndrome | n2=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | rel=r_associated | relid=0 | w=20 en:oculodental syndrome rutherfurd syndrome -- r_associated #0: 20 / 0.465 -> tylosis n1=en:oculodental syndrome rutherfurd syndrome | n2=tylosis | rel=r_associated | relid=0 | w=20

≈ 449 relations entrantes arachnodactylie --- r_associated #0: 190 --> en:oculodental syndrome rutherfurd syndrome n1=arachnodactylie | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=190 syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire --- r_associated #0: 188 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome héréditaire de prédisposition au cancer du sein et de l'ovaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=188 maladie de Marfan --- r_associated #0: 186 --> en:oculodental syndrome rutherfurd syndrome n1=maladie de Marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=186 syndrome de Marfan --- r_associated #0: 186 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de Marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=186 en:arachnodactyly --- r_associated #0: 184 --> en:oculodental syndrome rutherfurd syndrome n1=en:arachnodactyly | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=184 en:hereditary breast and ovarian cancer syndrome --- r_associated #0: 184 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary breast and ovarian cancer syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=184 syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire --- r_associated #0: 181 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de prédisposition héréditaire au cancer du sein et de l'ovaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=181 en:marfan syndrome --- r_associated #0: 171 --> en:oculodental syndrome rutherfurd syndrome n1=en:marfan syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=171 syndrome héréditaire de cancer du sein et de l'ovaire --- r_associated #0: 171 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome héréditaire de cancer du sein et de l'ovaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=171 neuropathie héréditaire sensitive et autonome de type i --- r_associated #0: 151 --> en:oculodental syndrome rutherfurd syndrome n1=neuropathie héréditaire sensitive et autonome de type i | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=151 neuropathie héréditaire sensitive et autonome de type 1 --- r_associated #0: 150 --> en:oculodental syndrome rutherfurd syndrome n1=neuropathie héréditaire sensitive et autonome de type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=150 neuropathie sensitive héréditaire dominante de type i --- r_associated #0: 150 --> en:oculodental syndrome rutherfurd syndrome n1=neuropathie sensitive héréditaire dominante de type i | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=150 en:hereditary sensory autonomic neuropathy, type 1 --- r_associated #0: 146 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary sensory autonomic neuropathy, type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=146 chondrodysplasie héréditaire déformante --- r_associated #0: 140 --> en:oculodental syndrome rutherfurd syndrome n1=chondrodysplasie héréditaire déformante | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=140 aclasie diaphysaire --- r_associated #0: 135 --> en:oculodental syndrome rutherfurd syndrome n1=aclasie diaphysaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=135 exostose héréditaire multiple --- r_associated #0: 135 --> en:oculodental syndrome rutherfurd syndrome n1=exostose héréditaire multiple | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=135 en:tylosis --- r_associated #0: 134 --> en:oculodental syndrome rutherfurd syndrome n1=en:tylosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=134 en:hereditary multiple exostoses --- r_associated #0: 133 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary multiple exostoses | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=133 maladie exostosante multiple --- r_associated #0: 130 --> en:oculodental syndrome rutherfurd syndrome n1=maladie exostosante multiple | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=130 tylosis --- r_associated #0: 130 --> en:oculodental syndrome rutherfurd syndrome n1=tylosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=130 chondrodysplasie déformante héréditaire --- r_associated #0: 125 --> en:oculodental syndrome rutherfurd syndrome n1=chondrodysplasie déformante héréditaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=125 démence fronto-temporale --- r_associated #0: 122 --> en:oculodental syndrome rutherfurd syndrome n1=démence fronto-temporale | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=122 en:frontotemporal dementia --- r_associated #0: 120 --> en:oculodental syndrome rutherfurd syndrome n1=en:frontotemporal dementia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=120 maladie ostéogénique --- r_associated #0: 120 --> en:oculodental syndrome rutherfurd syndrome n1=maladie ostéogénique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=120 en:lynch syndrome --- r_associated #0: 118 --> en:oculodental syndrome rutherfurd syndrome n1=en:lynch syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=118 démence frontotemporale --- r_associated #0: 115 --> en:oculodental syndrome rutherfurd syndrome n1=démence frontotemporale | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=115 en:Lynch syndrome --- r_associated #0: 115 --> en:oculodental syndrome rutherfurd syndrome n1=en:Lynch syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=115 maladie de Bessel-Hagen --- r_associated #0: 115 --> en:oculodental syndrome rutherfurd syndrome n1=maladie de Bessel-Hagen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=115 maladie des exostoses multiples --- r_associated #0: 110 --> en:oculodental syndrome rutherfurd syndrome n1=maladie des exostoses multiples | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=110 neuropathie sensitive héréditaire dominante de type I --- r_associated #0: 105 --> en:oculodental syndrome rutherfurd syndrome n1=neuropathie sensitive héréditaire dominante de type I | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=105 piébaldisme --- r_associated #0: 97 --> en:oculodental syndrome rutherfurd syndrome n1=piébaldisme | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=97 en:piebaldism --- r_associated #0: 95 --> en:oculodental syndrome rutherfurd syndrome n1=en:piebaldism | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=95 piebaldisme --- r_associated #0: 95 --> en:oculodental syndrome rutherfurd syndrome n1=piebaldisme | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=95 syndrome de Lynch --- r_associated #0: 81 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de Lynch | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=81 en:multiple osteogenic exostoses --- r_associated #0: 80 --> en:oculodental syndrome rutherfurd syndrome n1=en:multiple osteogenic exostoses | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=80 Cancer colorectal héréditaire sans polypose --- r_associated #0: 60 --> en:oculodental syndrome rutherfurd syndrome n1=Cancer colorectal héréditaire sans polypose | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=60 naevomatose baso-cellulaire --- r_associated #0: 56 --> en:oculodental syndrome rutherfurd syndrome n1=naevomatose baso-cellulaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=56 neurofibromatose de type 1 --- r_associated #0: 56 --> en:oculodental syndrome rutherfurd syndrome n1=neurofibromatose de type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=56 syndrome de Gorlin --- r_associated #0: 56 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de Gorlin | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=56 cancer colorectal héréditaire sans polypose --- r_associated #0: 55 --> en:oculodental syndrome rutherfurd syndrome n1=cancer colorectal héréditaire sans polypose | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=55 naevomatose basocellulaire --- r_associated #0: 54 --> en:oculodental syndrome rutherfurd syndrome n1=naevomatose basocellulaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=54 syndrome d'Alagille --- r_associated #0: 53 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome d'Alagille | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=53 en:Marfan's syndrome --- r_associated #0: 48 --> en:oculodental syndrome rutherfurd syndrome n1=en:Marfan's syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=48 en:hereditary nonpolyposis colorectal cancer --- r_associated #0: 48 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary nonpolyposis colorectal cancer | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=48 syndrome de marfan --- r_associated #0: 48 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=48 maladie clinique de recklinghausen --- r_associated #0: 47 --> en:oculodental syndrome rutherfurd syndrome n1=maladie clinique de recklinghausen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=47 maladie de Recklinghausen --- r_associated #0: 46 --> en:oculodental syndrome rutherfurd syndrome n1=maladie de Recklinghausen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=46 maladie de marfan --- r_associated #0: 46 --> en:oculodental syndrome rutherfurd syndrome n1=maladie de marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=46 maladie de von Recklinghausen --- r_associated #0: 46 --> en:oculodental syndrome rutherfurd syndrome n1=maladie de von Recklinghausen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=46 cancer colo-rectal héréditaire sans polypose --- r_associated #0: 45 --> en:oculodental syndrome rutherfurd syndrome n1=cancer colo-rectal héréditaire sans polypose | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=45 syndrome de douleur extrême paroxystique --- r_associated #0: 44 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de douleur extrême paroxystique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=44 en:kbg syndrome --- r_associated #0: 43 --> en:oculodental syndrome rutherfurd syndrome n1=en:kbg syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=43 en:keratosis palmoplantaris papulosa --- r_associated #0: 43 --> en:oculodental syndrome rutherfurd syndrome n1=en:keratosis palmoplantaris papulosa | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=43 en:craniosynostosis with facial dysmorphism and brachydactyly syndrome --- r_associated #0: 42 --> en:oculodental syndrome rutherfurd syndrome n1=en:craniosynostosis with facial dysmorphism and brachydactyly syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=42 en:reis-bucklers' corneal dystrophy --- r_associated #0: 42 --> en:oculodental syndrome rutherfurd syndrome n1=en:reis-bucklers' corneal dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=42 en:von Recklinghausen's disease --- r_associated #0: 42 --> en:oculodental syndrome rutherfurd syndrome n1=en:von Recklinghausen's disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=42 en:neurofibromatosis type 1 --- r_associated #0: 41 --> en:oculodental syndrome rutherfurd syndrome n1=en:neurofibromatosis type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=41 en:paroxysmal extreme pain disorder --- r_associated #0: 41 --> en:oculodental syndrome rutherfurd syndrome n1=en:paroxysmal extreme pain disorder | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=41 en:shprintzen omphalocele syndrome --- r_associated #0: 41 --> en:oculodental syndrome rutherfurd syndrome n1=en:shprintzen omphalocele syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=41 dysplasie cléido-crânienne --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=dysplasie cléido-crânienne | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 dysplasie cléidocrânienne --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=dysplasie cléidocrânienne | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 en:Pitt-Hopkins syndrome --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=en:Pitt-Hopkins syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 en:charcot-marie-tooth disease, axonal, type 2e (disorder) --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=en:charcot-marie-tooth disease, axonal, type 2e (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 en:jackson-weiss syndrome --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=en:jackson-weiss syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 en:spinocerebellar ataxia 1s --- r_associated #0: 40 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 1s | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=40 en:Feingold syndrome --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:Feingold syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:advanced sleep-phase syndrome, familial --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:advanced sleep-phase syndrome, familial | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:centronuclear myopathy 1 --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:centronuclear myopathy 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:cleidocranial dysplasia --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:cleidocranial dysplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:epiphyseal dysplasia, multiple, 1 --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:epiphyseal dysplasia, multiple, 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:familial isolated arrhythmogenic right ventricular dysplasia --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial isolated arrhythmogenic right ventricular dysplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:keratoacanthoma familial --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:keratoacanthoma familial | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:nevoid basal cell carcinoma syndrome --- r_associated #0: 39 --> en:oculodental syndrome rutherfurd syndrome n1=en:nevoid basal cell carcinoma syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=39 en:cochleosaccular degeneration of the inner ear and progressive cataracts --- r_associated #0: 38 --> en:oculodental syndrome rutherfurd syndrome n1=en:cochleosaccular degeneration of the inner ear and progressive cataracts | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=38 en:dopa-responsive dystonia --- r_associated #0: 38 --> en:oculodental syndrome rutherfurd syndrome n1=en:dopa-responsive dystonia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=38 en:okihiro syndrome --- r_associated #0: 38 --> en:oculodental syndrome rutherfurd syndrome n1=en:okihiro syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=38 exostosante (maladie) --- r_associated #0: 38 --> en:oculodental syndrome rutherfurd syndrome n1=exostosante (maladie) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=38 en:autosomal dominant deficiency of plasminogen --- r_associated #0: 37 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant deficiency of plasminogen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=37 en:dyskeratosis congenita, autosomal dominant --- r_associated #0: 37 --> en:oculodental syndrome rutherfurd syndrome n1=en:dyskeratosis congenita, autosomal dominant | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=37 en:dystrophia myotonica 2 --- r_associated #0: 37 --> en:oculodental syndrome rutherfurd syndrome n1=en:dystrophia myotonica 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=37 en:feingold syndrome --- r_associated #0: 37 --> en:oculodental syndrome rutherfurd syndrome n1=en:feingold syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=37 en:behavioral variant of frontotemporal dementia --- r_associated #0: 36 --> en:oculodental syndrome rutherfurd syndrome n1=en:behavioral variant of frontotemporal dementia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=36 en:spinocerebellar ataxia 28 --- r_associated #0: 36 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 28 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=36 goniodysgénésie-retard mental-petite taille (syndrome) --- r_associated #0: 36 --> en:oculodental syndrome rutherfurd syndrome n1=goniodysgénésie-retard mental-petite taille (syndrome) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=36 nævomatose basocellulaire multiple --- r_associated #0: 36 --> en:oculodental syndrome rutherfurd syndrome n1=nævomatose basocellulaire multiple | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=36 stomatocytose héréditaire --- r_associated #0: 36 --> en:oculodental syndrome rutherfurd syndrome n1=stomatocytose héréditaire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=36 en:aniridia and intellectual disability syndrome --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:aniridia and intellectual disability syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:aplasia of lacrimal and salivary glands --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:aplasia of lacrimal and salivary glands | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant idiopathic familial dystonia --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant idiopathic familial dystonia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:autosomal dominant muscular dystrophy not predominantly limb girdle --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant muscular dystrophy not predominantly limb girdle | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:brooke-spiegler syndrome --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:brooke-spiegler syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:capillary malformation-arteriovenous malformation (disorder) --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:capillary malformation-arteriovenous malformation (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:congenital nephrogenic diabetes insipidus --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:congenital nephrogenic diabetes insipidus | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:dominant autosomal hereditary disorder, complete penetrance --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:dominant autosomal hereditary disorder, complete penetrance | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:dominant autosomal hereditary disorder, incomplete penetrance --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:dominant autosomal hereditary disorder, incomplete penetrance | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:episodic ataxia --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:episodic ataxia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:familial benign neonatal epilepsy --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial benign neonatal epilepsy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:fibrodysplasia ossificans progressiva --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:fibrodysplasia ossificans progressiva | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:goniodysgenesis-mental retardation-short stature syndrome --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:goniodysgenesis-mental retardation-short stature syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:hereditary elliptocytosis due to abnormal protein 4.1 --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary elliptocytosis due to abnormal protein 4.1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome --- r_associated #0: 35 --> 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:hyperferritinemia, hereditary, with congenital cataracts --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperferritinemia, hereditary, with congenital cataracts | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:hyperinsulinism due to hnf1a deficiency --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinism due to hnf1a deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:hyperpigmentation, familial progressive --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperpigmentation, familial progressive | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:neurofibromatosis type 2 --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:neurofibromatosis type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:polydactyly, preaxial ii (disorder) --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:polydactyly, preaxial ii (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:roch leri mesosomatous lipomatosis --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:roch leri mesosomatous lipomatosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:sebastian syndrome --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:sebastian syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:spinocerebellar ataxia type 2 --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:transthyretin related familial amyloid cardiomyopathy --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:transthyretin related familial amyloid cardiomyopathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 en:wnt4 mullerian aplasia and ovarian dysfunction --- r_associated #0: 35 --> en:oculodental syndrome rutherfurd syndrome n1=en:wnt4 mullerian aplasia and ovarian dysfunction | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=35 dysplasie acromicrique --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=dysplasie acromicrique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 dystonie dopasensible --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=dystonie dopasensible | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:17q11.2 microduplication syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:17q11.2 microduplication syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:ameloonychohypohidrotic syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:ameloonychohypohidrotic syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant analbuminemia --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant analbuminemia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant charcot-marie-tooth disease type 2m --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2m | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant focal dystonia dyt25 type --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant focal dystonia dyt25 type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant hyperinsulinism due to kir6.2 deficiency --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant hyperinsulinism due to kir6.2 deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant ichthyosis --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant ichthyosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:autosomal dominant oculocutaneous albinism --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant oculocutaneous albinism | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:bilateral pheochromocytoma and islet cell adenoma of the pancreas --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:bilateral pheochromocytoma and islet cell adenoma of the pancreas | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:cardiac anomaly and heterotaxy syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:cardiac anomaly and heterotaxy syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:cataract glaucoma syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:cataract glaucoma syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:dysplasia, saddan --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:dysplasia, saddan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:familial encephalopathy with neuroserpin inclusion bodies --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial encephalopathy with neuroserpin inclusion bodies | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:familial hemiplegic migraine --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial hemiplegic migraine | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:familial osteochondritis dissecans --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial osteochondritis dissecans | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:haspeslagh fryns muelenaere syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:haspeslagh fryns muelenaere syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:heritable pulmonary arterial hypertension due to bmpr2 mutation --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:heritable pulmonary arterial hypertension due to bmpr2 mutation | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:hyperinsulinemic hypoglycemia, familial, 7 --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinemic hypoglycemia, familial, 7 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:leopard syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:leopard syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:microphthalmia, syndromic 3 --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:microphthalmia, syndromic 3 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:mowat-wilson syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:mowat-wilson syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:muckle-wells syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:muckle-wells syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:noonan syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:noonan syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:osteogenesis imperfecta, levin type --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:osteogenesis imperfecta, levin type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:pitt-hopkins syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:pitt-hopkins syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:spinocerebellar ataxia 31 (disorder) --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 31 (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:spinocerebellar ataxia type 37 --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 37 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:spondyloperipheral dysplasia short ulna --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:spondyloperipheral dysplasia short ulna | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:ulna metaphyseal dysplasia syndrome --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:ulna metaphyseal dysplasia syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:vitreoretinochoroidopathy (disorder) --- r_associated #0: 34 --> en:oculodental syndrome rutherfurd syndrome n1=en:vitreoretinochoroidopathy (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=34 en:hereditary non polyposis colorectal cancer --- r_associated #0: 33 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary non polyposis colorectal cancer | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=33 en:hereditary stomatocytosis --- r_associated #0: 33 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary stomatocytosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=33 Syndrome de Marfan --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=Syndrome de Marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:Marfan's disease --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:Marfan's disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:acromicric dysplasia --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:acromicric dysplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant ichthyosis vulgaris --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant ichthyosis vulgaris | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant palmoplantar keratoderma and congenital alopecia --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant palmoplantar keratoderma and congenital alopecia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:autosomal dominant progressive nephropathy with hypertension --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant progressive nephropathy with hypertension | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:basal cell nevus syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:basal cell nevus syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:chromosome 22q11.2 microduplication syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:chromosome 22q11.2 microduplication syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:deafness-craniofacial syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:deafness-craniofacial syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:diffuse palmoplantar keratoderma and acrocyanosis syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:diffuse palmoplantar keratoderma and acrocyanosis syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:dominant beta-thalassemia --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:dominant beta-thalassemia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:familial hypodontia --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial hypodontia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:familial non-autoimmune autosomal dominant hyperthyroidism --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial non-autoimmune autosomal dominant hyperthyroidism | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:frontotemporal dementia, chromosome 3-linked --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:frontotemporal dementia, chromosome 3-linked | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:frontotemporal lobar degeneration with tdp43 inclusions, grn-related | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:hereditary mucosal leukokeratosis --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary mucosal leukokeratosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:hereditary myopathy with early respiratory failure --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary myopathy with early respiratory failure | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:laurin-sandrow syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:laurin-sandrow syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:li-fraumeni syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:li-fraumeni syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:melnick-fraser syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:melnick-fraser syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:microcephaly deafness syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:microcephaly deafness syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:myopathy, distal, tateyama type --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:myopathy, distal, tateyama type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:potocki-shaffer syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:potocki-shaffer syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:pseudohypoaldosteronism, type 1, dominant form --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:pseudohypoaldosteronism, type 1, dominant form | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:short stature with valvular heart disease and characteristic facies syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:short stature with valvular heart disease and characteristic facies syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:spinocerebellar ataxia 10 --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 10 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:spinocerebellar ataxia 29 --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 29 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:spinocerebellar ataxia 36 --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 36 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:spinocerebellar ataxia 8 --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia 8 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:spondylocostal dysostosis 4, autosomal dominant --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:spondylocostal dysostosis 4, autosomal dominant | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:tarsal-carpal coalition syndrome --- r_associated #0: 32 --> en:oculodental syndrome rutherfurd syndrome n1=en:tarsal-carpal coalition syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=32 en:Lynch'syndrome --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:Lynch'syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:alpha-fetoprotein, hereditary persistence of --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:alpha-fetoprotein, hereditary persistence of | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:brachymesophalangy 2 and 5 --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:brachymesophalangy 2 and 5 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:brachyolmia type 3 --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:brachyolmia type 3 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:charcot-marie-tooth disease type 2d --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:charcot-marie-tooth disease type 2d | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:cleidorhizomelic syndrome --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:cleidorhizomelic syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:congenital reticular ichthyosiform erythroderma --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:congenital reticular ichthyosiform erythroderma | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:corneal dystrophy, subepithelial mucinous --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:corneal dystrophy, subepithelial mucinous | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:czech dysplasia, metatarsal type --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:czech dysplasia, metatarsal type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:dentatorubral-pallidoluysian atrophy --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:dentatorubral-pallidoluysian atrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:ectodermal dysplasia with natal teeth, turnpenny type --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:ectodermal dysplasia with natal teeth, turnpenny type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:hyperinsulinemic hypoglycemia, familial, 6 --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinemic hypoglycemia, familial, 6 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:iris coloboma with ptosis, hypertelorism, and mental retardation --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:iris coloboma with ptosis, hypertelorism, and mental retardation | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:lamellar ichthyosis, autosomal dominant form --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:lamellar ichthyosis, autosomal dominant form | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:mild spondyloepiphyseal dysplasia due to col2a1 mutation with early onset osteoarthritis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:pituitary adenoma, familial isolated (disorder) --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:pituitary adenoma, familial isolated (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:potassium aggravated myotonia --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:potassium aggravated myotonia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:preaxial deficiency, postaxial polydactyly and hypospadias --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:preaxial deficiency, postaxial polydactyly and hypospadias | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:proteus-like syndrome (disorder) --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:proteus-like syndrome (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:reticulate acropigmentation of kitamura --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:reticulate acropigmentation of kitamura | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:spinocerebellar ataxia type 32 --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 32 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 en:type v acrocephalosyndactyly --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=en:type v acrocephalosyndactyly | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 migraine hémiplégique familiale --- r_associated #0: 31 --> en:oculodental syndrome rutherfurd syndrome n1=migraine hémiplégique familiale | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=31 Syndrome d'Alagille --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=Syndrome d'Alagille | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 Syndrome de Gorlin --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=Syndrome de Gorlin | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:acro-dermato-ungual-lacrimal-tooth syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:acro-dermato-ungual-lacrimal-tooth syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant charcot-marie-tooth disease type 2a1 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2a1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant charcot-marie-tooth disease type 2c --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant charcot-marie-tooth disease type 2c | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant familial woolly hair --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant familial woolly hair | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant inheritance --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant inheritance | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant mutilating keratoderma --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant mutilating keratoderma | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant pterygium of conjunctiva --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant pterygium of conjunctiva | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:autosomal dominant retinitis pigmentosa --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant retinitis pigmentosa | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:basal cell nævus --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:basal cell nævus | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:bethlem myopathy 1 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:bethlem myopathy 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:brachydactyly type a6 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:brachydactyly type a6 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:brachydactyly, type a1 (disorder) --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:brachydactyly, type a1 (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:charcot-marie-tooth disease, axonal, type 2b (disorder) --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:charcot-marie-tooth disease, axonal, type 2b (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:charcot-marie-tooth disease, axonal, type 2l (disorder) --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:charcot-marie-tooth disease, axonal, type 2l (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:charcot-marie-tooth disease, type 2j --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:charcot-marie-tooth disease, type 2j | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:chromosome 17q21.31 deletion syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:chromosome 17q21.31 deletion syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:crouzon syndrome with acanthosis nigricans (disorder) --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:crouzon syndrome with acanthosis nigricans (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:epilepsy, myoclonic, benign adult familial, type 2 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:epilepsy, myoclonic, benign adult familial, type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:generalized myotonia of thomsen --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:generalized myotonia of thomsen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:glucose transporter protein type 1 deficiency syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:glucose transporter protein type 1 deficiency syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:hereditary cerebral amyloid angiopathy, icelandic type --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary cerebral amyloid angiopathy, icelandic type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:hereditary gastrogenic lactose intolerance --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary gastrogenic lactose intolerance | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:hereditary sensory and autonomic neuropathy type 1b --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary sensory and autonomic neuropathy type 1b | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:hyaline dystrophy of bruch's membrane --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyaline dystrophy of bruch's membrane | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:hypoplastic tibia and postaxial polydactyly syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:hypoplastic tibia and postaxial polydactyly syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:may-hegglin anomaly --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:may-hegglin anomaly | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:mesomelic dwarfism reinhardt pfeiffer type --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:mesomelic dwarfism reinhardt pfeiffer type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:multiple endocrine neoplasia type 2b --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:multiple endocrine neoplasia type 2b | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:multiple epiphyseal dysplasia type 5 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:multiple epiphyseal dysplasia type 5 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:myopathy, distal 2 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:myopathy, distal 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:parietal foramina --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:parietal foramina | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:spinocerebellar ataxia type 4 --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 4 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:steatocystoma multiplex --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:steatocystoma multiplex | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:tubular renal disease with cardiomyopathy syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:tubular renal disease with cardiomyopathy syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:ulnar-mammary syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:ulnar-mammary syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:vitelliform macular dystrophy --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:vitelliform macular dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 en:zimmerman laband syndrome --- r_associated #0: 30 --> en:oculodental syndrome rutherfurd syndrome n1=en:zimmerman laband syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=30 Marfan (maladie de) --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=Marfan (maladie de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:Alagille's syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:Alagille's syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:Bessel-Hagen's disease --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:Bessel-Hagen's disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - rough | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:arthrogryposis, distal, type 1 --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:arthrogryposis, distal, type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:autosomal dominant beta2-microglobulinic amyloidosis --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant beta2-microglobulinic amyloidosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:avascular necrosis of femoral head --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:avascular necrosis of femoral head | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:blau syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:blau syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:dicer1 syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:dicer1 syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:dyschondrosteosis and nephritis syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:dyschondrosteosis and nephritis syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:dystonia 12 --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:dystonia 12 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:glomuvenous malformations --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:glomuvenous malformations | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:hawkinsinuria --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:hawkinsinuria | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:hereditary motor and sensory neuropathy type i --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary motor and sensory neuropathy type i | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:hyperinsulinism due to deficiency of glucokinase --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinism due to deficiency of glucokinase | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:hyperinsulinism due to uncoupling protein 2 deficiency --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinism due to uncoupling protein 2 deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:loeys-dietz syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:loeys-dietz syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:morava mehes syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:morava mehes syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:neuropathy, hereditary thermosensitive --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:neuropathy, hereditary thermosensitive | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:nicolaides baraitser syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:nicolaides baraitser syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:turcot syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:turcot syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 en:wellesley carman french syndrome --- r_associated #0: 29 --> en:oculodental syndrome rutherfurd syndrome n1=en:wellesley carman french syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=29 Lynch (syndrome de) --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=Lynch (syndrome de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:alagille syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:alagille syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:amelogenesis imperfecta - hypoplastic autosomal dominant - smooth | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:andersen syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:andersen syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:aniridia, ptosis, intellectual disability, familial obesity syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:aniridia, ptosis, intellectual disability, familial obesity syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:aphalangy and syndactyly with microcephaly syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:aphalangy and syndactyly with microcephaly syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:autoimmune lymphoproliferative syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:autoimmune lymphoproliferative syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant excess of transthyretin --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant excess of transthyretin | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:autosomal dominant variant form of albumin --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant variant form of albumin | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:cataract, congenital, cerulean type 1 --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:cataract, congenital, cerulean type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:cerebral hemorrhage with amyloidosis, hereditary, dutch type --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:cerebral hemorrhage with amyloidosis, hereditary, dutch type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:char syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:char syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:chromosome 3q29 deletion syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:chromosome 3q29 deletion syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:cole disease --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:cole disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:congenital dyserythropoietic anemia, type iii --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:congenital dyserythropoietic anemia, type iii | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:epithelial recurrent erosion dystrophy --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:epithelial recurrent erosion dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:familial spontaneous pneumothorax --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial spontaneous pneumothorax | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:geniospasm 1 --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:geniospasm 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:gingival hypertrophy --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:gingival hypertrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:hereditary papillary renal cell carcinoma --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary papillary renal cell carcinoma | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:hereditary systemic amyloidosis --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary systemic amyloidosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:hnsha due to triosephosphate isomerase deficiency --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:hnsha due to triosephosphate isomerase deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:hyperparathyroidism-jaw tumor syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperparathyroidism-jaw tumor syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:hypertrichosis terminalis, generalized, with or without gingival hyperplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:liddle syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:liddle syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:marfan's syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:marfan's syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:nemaline myopathy 3 --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:nemaline myopathy 3 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:peutz-jeghers syndrome --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:peutz-jeghers syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:primary pigmented nodular adrenocortical disease --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:primary pigmented nodular adrenocortical disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:radial hypoplasia, triphalangeal thumbs and hypospadias --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:radial hypoplasia, triphalangeal thumbs and hypospadias | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:spinocerebellar ataxia type 7 --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 7 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:sting-associated vasculopathy with onset in infancy --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:sting-associated vasculopathy with onset in infancy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:syndrome, branchio-oculo-facial --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:syndrome, branchio-oculo-facial | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:thiel-behnke corneal dystrophy --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=en:thiel-behnke corneal dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 syndrome d'alagille --- r_associated #0: 28 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome d'alagille | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=28 en:absence of fingerprints with congenital milia syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:absence of fingerprints with congenital milia syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:auriculo-condylar syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:auriculo-condylar syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:beare-stevenson cutis gyrata syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:beare-stevenson cutis gyrata syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:cerebral cavernous malformation --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:cerebral cavernous malformation | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:currarino triad --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:currarino triad | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:familial partial lipodystrophy, type 2 --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial partial lipodystrophy, type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:generalized epilepsy and paroxysmal dyskinesia syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:generalized epilepsy and paroxysmal dyskinesia syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:gracile bone dysplasia --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:gracile bone dysplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:hereditary cystatin c amyloid angiopathy --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary cystatin c amyloid angiopathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:hyperuricemia, anemia, renal failure syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperuricemia, anemia, renal failure syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:hypotrichosis simplex of scalp --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:hypotrichosis simplex of scalp | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:short fifth metacarpal insulin resistance syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:short fifth metacarpal insulin resistance syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:spinocerebellar ataxia type 5 --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 5 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:steinfeld syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:steinfeld syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:strudwick syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:strudwick syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:synpolydactyly --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:synpolydactyly | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:treacher collins syndrome --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=en:treacher collins syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 syndrome de gorlin --- r_associated #0: 27 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de gorlin | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=27 en:autosomal dominant hyperinsulinism due to sur1 deficiency --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant hyperinsulinism due to sur1 deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant hypophosphatemic bone disease --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant hypophosphatemic bone disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:autosomal dominant optic atrophy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant optic atrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:bannayan syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:bannayan syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:benign autosomal dominant osteopetrosis --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:benign autosomal dominant osteopetrosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:bilateral multiple fibroadenoma of breast --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:bilateral multiple fibroadenoma of breast | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:brachytelephalangy, facial dysmorphism, kallmann syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:brachytelephalangy, facial dysmorphism, kallmann syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:cap myopathy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:cap myopathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:choreoathetosis/spasticity, episodic --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:choreoathetosis/spasticity, episodic | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:corneal dystrophy, congenital stromal --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:corneal dystrophy, congenital stromal | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:craniofacial deafness hand syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:craniofacial deafness hand syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:ehlers-danlos syndrome vascular-like type --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:ehlers-danlos syndrome vascular-like type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:epiphyseal dysplasia, multiple, 2 --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:epiphyseal dysplasia, multiple, 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:familial amyloid neuropathy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial amyloid neuropathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:familial creutzfeldt-jakob --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial creutzfeldt-jakob | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:familial digital arthropathy and brachydactyly syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial digital arthropathy and brachydactyly syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hand foot uterus syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hand foot uterus syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary angioedema --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary angioedema | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary corneal dystrophy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary corneal dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary diffuse gastric adenocarcinoma --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary diffuse gastric adenocarcinoma | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary elliptocytosis due to alpha spectrin defect --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary elliptocytosis due to alpha spectrin defect | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary elliptocytosis due to beta spectrin defect in self-association --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary elliptocytosis due to beta spectrin defect in self-association | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hereditary oculoleptomeningeal amyloid angiopathy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary oculoleptomeningeal amyloid angiopathy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hyperinsulinism due to hnf4a deficiency --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinism due to hnf4a deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:hyperinsulinism due to insulin receptor deficiency --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:hyperinsulinism due to insulin receptor deficiency | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:melanoma astrocytoma syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:melanoma astrocytoma syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:metaphyseal dysplasia, braun-tinschert type --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:metaphyseal dysplasia, braun-tinschert type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:microcornea with glaucoma and absent frontal sinus syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:microcornea with glaucoma and absent frontal sinus syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:neurofibromatosis, type 1-like syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:neurofibromatosis, type 1-like syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:neuropathy, hereditary motor and sensory, okinawa type --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:neuropathy, hereditary motor and sensory, okinawa type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:peripheral resistance to thyroid hormone --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:peripheral resistance to thyroid hormone | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:piussan lenaerts mathieu syndrome --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:piussan lenaerts mathieu syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:schnyder crystalline corneal dystrophy --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:schnyder crystalline corneal dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:spinocerebellar ataxia type 6 (disorder) --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:spinocerebellar ataxia type 6 (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:split-hand-foot malformation with long bone deficiency 1 --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:split-hand-foot malformation with long bone deficiency 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:syndactyly, type i --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:syndactyly, type i | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:syndactyly, type iii --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:syndactyly, type iii | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:syndromic orbital border hypoplasia --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:syndromic orbital border hypoplasia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:timothy syndrome type 2 --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:timothy syndrome type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:type i acrocephalosyndactyly --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:type i acrocephalosyndactyly | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 en:whyte hemingway carpal tarsal phalangeal osteolyses --- r_associated #0: 26 --> en:oculodental syndrome rutherfurd syndrome n1=en:whyte hemingway carpal tarsal phalangeal osteolyses | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=26 corne cutanée de la paupière --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=corne cutanée de la paupière | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:adult onset autosomal dominant leukodystrophy --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:adult onset autosomal dominant leukodystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:autosomal dominant epidermolysis bullosa simplex --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant epidermolysis bullosa simplex | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:autosomal dominant late onset basal ganglia degeneration --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant late onset basal ganglia degeneration | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:familial hypercalciuric hypocalcemia --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:familial hypercalciuric hypocalcemia | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:hereditary motor and sensory neuropathy type I --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary motor and sensory neuropathy type I | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:hereditary multiple ossifying ecchondromata --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary multiple ossifying ecchondromata | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:mullerian duct and limb anomalies syndrome --- r_associated #0: 25 --> en:oculodental syndrome rutherfurd syndrome n1=en:mullerian duct and limb anomalies syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=25 en:amelogenesis imperfecta, type ib --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:amelogenesis imperfecta, type ib | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:atelosteogenesis, type 1 --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:atelosteogenesis, type 1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:corneal dystrophy --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:corneal dystrophy | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:delayed eruption of primary teeth --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:delayed eruption of primary teeth | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:ehlers-danlos syndrome, type i --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:ehlers-danlos syndrome, type i | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:failure of secondary teeth eruption --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:failure of secondary teeth eruption | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:sellars beighton syndrome --- r_associated #0: 24 --> en:oculodental syndrome rutherfurd syndrome n1=en:sellars beighton syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=24 en:acrodysostosis --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:acrodysostosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:acute intermittent porphyria --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:acute intermittent porphyria | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:corneal haze --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:corneal haze | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:hereditary benign intraepithelial dyskeratosis --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary benign intraepithelial dyskeratosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:insulin autoimmune syndrome --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:insulin autoimmune syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:keratitis, hereditary --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:keratitis, hereditary | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:popliteal pterygium syndrome --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=en:popliteal pterygium syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 tylose --- r_associated #0: 23 --> en:oculodental syndrome rutherfurd syndrome n1=tylose | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=23 en:Gorlin syndrome --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:Gorlin syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:arachnodactily --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:arachnodactily | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:autosomal dominant cystoid macular edema --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant cystoid macular edema | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:autosomal dominant polycystic kidney disease --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:autosomal dominant polycystic kidney disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:cutis laxa, autosomal dominant --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:cutis laxa, autosomal dominant | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:freeman-sheldon syndrome --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:freeman-sheldon syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:genitopatellar syndrome --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:genitopatellar syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:hereditary elliptocytosis due to deficiency of protein 4.1 --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:hereditary elliptocytosis due to deficiency of protein 4.1 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:von willebrand disease, platelet type --- r_associated #0: 22 --> en:oculodental syndrome rutherfurd syndrome n1=en:von willebrand disease, platelet type | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=22 en:dentin dyspalsia, shields type 2 --- r_associated #0: 21 --> en:oculodental syndrome rutherfurd syndrome n1=en:dentin dyspalsia, shields type 2 | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=21 en:foxg1 syndrome --- r_associated #0: 21 --> en:oculodental syndrome rutherfurd syndrome n1=en:foxg1 syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=21 en:LEOPARD syndrome --- r_associated #0: 20 --> en:oculodental syndrome rutherfurd syndrome n1=en:LEOPARD syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=20 syndrome --- r_associated #0: 20 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=20 Maladie de Marfan --- r_associated #0: 15 --> en:oculodental syndrome rutherfurd syndrome n1=Maladie de Marfan | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=15 Syndrome de Lynch --- r_associated #0: 15 --> en:oculodental syndrome rutherfurd syndrome n1=Syndrome de Lynch | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=15 démence (sémiologie) --- r_associated #0: 15 --> en:oculodental syndrome rutherfurd syndrome n1=démence (sémiologie) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=15 en:tylose --- r_associated #0: 15 --> en:oculodental syndrome rutherfurd syndrome n1=en:tylose | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=15 Bessel-Hagen (maladie de) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=Bessel-Hagen (maladie de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 Gorlin (syndrome de) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=Gorlin (syndrome de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 MIGP (orientation) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=MIGP (orientation) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 Recklinghausen (maladie de von) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=Recklinghausen (maladie de von) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 Recklinghausen (neurofibromatose de) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=Recklinghausen (neurofibromatose de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 Tylosis --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=Tylosis | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 absence d'empreintes digitales avec syndrome de milia congénital --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=absence d'empreintes digitales avec syndrome de milia congénital | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 angl. HNPCC --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=angl. HNPCC | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 en:Peutz-Jeghers syndrome --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=en:Peutz-Jeghers syndrome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 en:von recklinghausen's disease --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=en:von recklinghausen's disease | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 exostose du conduit auditif externe --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=exostose du conduit auditif externe | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 exostose ostéocartilagineuse --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=exostose ostéocartilagineuse | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 exostose sous-unguéale --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=exostose sous-unguéale | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 exostosectomie --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=exostosectomie | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 goniome --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=goniome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 goniomètre --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=goniomètre | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonion --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonion | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonioscopie --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonioscopie | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 goniosynéchies --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=goniosynéchies | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 goniotomie endoscopique --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=goniotomie endoscopique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonochorisme --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonochorisme | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonococcie --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonococcie | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonocoque --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonocoque | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonocyte --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonocyte | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonocytome --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonocytome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonométrie --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonométrie | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonorrhée --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonorrhée | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonosome --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonosome | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 gonosomique --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=gonosomique | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 neurofibromatose de Recklinghausen --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=neurofibromatose de Recklinghausen | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 neuropathie sensitivomotrice héréditaire forme I --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=neuropathie sensitivomotrice héréditaire forme I | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 paraplégie spastique dans la syphilis congénitale --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=paraplégie spastique dans la syphilis congénitale | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 steatocystoma multiplex --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=steatocystoma multiplex | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 stéatocystomes multiples --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=stéatocystomes multiples | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 syndrome d'hyperparathyroïdie et tumeur de la mâchoire --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome d'hyperparathyroïdie et tumeur de la mâchoire | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 syndrome de Feingold --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de Feingold | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 syndrome de Pitt-Hopkins --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome de Pitt-Hopkins | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 ty (élément) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=ty (élément) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 von Recklinghausen (maladie de) --- r_associated #0: 10 --> en:oculodental syndrome rutherfurd syndrome n1=von Recklinghausen (maladie de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=10 Alagille (syndrome d') --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=Alagille (syndrome d') | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 Stokvis-Talma (syndrome de) --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=Stokvis-Talma (syndrome de) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 démence d'Alzheimer --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=démence d'Alzheimer | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 lynestrénol --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=lynestrénol | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 lyo-enzyme --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=lyo-enzyme | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 lyoglycogène --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=lyoglycogène | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 nævique irien (syndrome) --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=nævique irien (syndrome) | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5 syndrome lymphoprolifératif avec autoimmunité --- r_associated #0: 5 --> en:oculodental syndrome rutherfurd syndrome n1=syndrome lymphoprolifératif avec autoimmunité | n2=en:oculodental syndrome rutherfurd syndrome | rel=r_associated | relid=0 | w=5