Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital cataract with deafness and hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital cataract with hypertrichosis and intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital cataract, nephropathy, encephalopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Cataract and microcornea syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital hereditary facial paralysis with variable hearing loss syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Oculogastrointestinal muscular dystrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Glaucoma, ectopia, microspherophakia, stiff joint, short stature syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Juvenile cataract, microcornea, renal glucosuria syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Matthew Wood syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Ectodermal dysplasia with blindness syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Severe X-linked intellectual disability Gustavson type (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Duane anomaly, myopathy, scoliosis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Ectopia lentis, chorioretinal dystrophy, myopia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Macular coloboma, cleft palate, hallux valgus syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Hypotrichosis with juvenile macular degeneration syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Macrostomia, preauricular tag, external ophthalmoplegia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Microbrachycephaly, ptosis, cleft lip syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Aplasia cutis congenita with epibulbar dermoid syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Syndactyly, telecanthus, anogenital and renal malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Multifocal pattern dystrophy of retinal pigment epithelium simulating fundus flavimaculatus (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome de lipomes naso-palpébraux-colobome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
X-linked spastic paraplegia type 2 (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Pigmented paravenous retinochoroidal atrophy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Revesz syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Pierson syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Ring dermoid of cornea (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Retinal degeneration, nanophthalmos, glaucoma syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Helicoid peripapillary chorioretinal degeneration (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Macrocephaly, obesity, mental disability, ocular abnormality syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Hypospadias, hypertelorism, coloboma, deafness syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome d'ataxie cérébelleuse, déficience intellectuelle, atrophie optique, anomalies cutanées |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Isolated optic nerve hypoplasia (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome de ptosis-strabisme-pupilles ectopiques |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Cortical blindness, intellectual disability, polydactyly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital cataract ichthyosis syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Epilepsy telangiectasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Hemifacial hyperplasia strabismus syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Duplication of eyebrow and syndactyly syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Spastic paraplegia, glaucoma, intellectual disability syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Pseudoprogeria syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Polydactyly myopia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Preaxial polydactyly, colobomata, intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Aniridia, renal agenesis, psychomotor retardation syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Megalocornea with intellectual disability syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Isolated congenital megalocornea (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Disorder of eye co-occurrent and due to Marfan syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome rein-colobome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome de cardiopathie, blépharophimosis, anomalie du radius, anomalie anale |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome de mèches blanches et anomalies multiples |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Spastic ataxia with congenital miosis |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Intellectual disability, alacrima, achalasia syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
syndrome oculo-auriculaire type Schorderet |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Oculopharyngodistal myopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Retinal arterial macroaneurysm with supravalvular pulmonic stenosis |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Familial isolated trichomegaly |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Progressive external ophthalmoplegia, myopathy, emaciation syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Moebius syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
fundus pulverulentus |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
X-linked cerebral, cerebellar, coloboma syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Congenital Horner syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
dysplasie pilo-dentaire |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Polymicrogyria with optic nerve hypoplasia |
est un(e) (attribut) |
False |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Ptosis and vocal cord paralysis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|
Spinal atrophy, ophthalmoplegia, pyramidal syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of the visual system |
Inferred relationship |
Some |
|