Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Myoclonus, cerebellar ataxia, deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Deafness, vitiligo, achalasia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Deafness, small bowel diverticulosis, neuropathy syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Spastic paraplegia, nephritis, deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Wolfram-like syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Retinitis pigmentosa-deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cleft palate, large ears, small head syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Facial dysmorphism, conductive hearing loss, heart defect syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Keipert syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Oculoauricular syndrome Schorderet type |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Postlingual non-syndromic genetic deafness |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Prelingual non-syndromic genetic deafness |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Branchiootic syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Waardenburg syndrome |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Alstrom syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Otopalatodigital syndrome |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Alport syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital deafness with labyrinthine aplasia, microtia and microdontia |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Sinoatrial node dysfunction and deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Mandibular hypoplasia, deafness, progeroid syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Ocular albinism with congenital sensorineural deafness |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Chudley McCullough syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Flat face, microstomia, ear anomaly syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Deafness with onychodystrophy syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital cataract, hearing loss, severe developmental delay syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Temtamy preaxial brachydactyly syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant aplasia and myelodysplasia |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Gemignani syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Stickler syndrome type 3 |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Familial steroid-resistant nephrotic syndrome with sensorineural deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hypotrichosis and deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
External auditory canal atresia, vertical talus, hypertelorism syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Oto-palato-digital syndrome, type I |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Oto-palato-digital syndrome, type II |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Pendred's syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Prune belly syndrome with pulmonic stenosis, intellectual disability and deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Fatal X-linked ataxia with deafness and loss of vision |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Inherited cochlear degeneration |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hystrix ichthyosis with deafness |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Multiple epiphyseal dysplasia Beighton type |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Johnson neuroectodermal syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary hearing loss |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Melnick-Fraser syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Renal tubular acidosis with progressive nerve deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
X-linked spinocerebellar ataxia type 3 |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Keratitis ichthyosis and deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Familial amyloid nephropathy with urticaria AND deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Albinism-deafness syndrome of Tietz |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Diabetes mellitus AND insipidus with optic atrophy AND deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Craniofacial deafness hand syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Emberger syndrome |
Is a |
False |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Progressive bulbar palsy with sensorineural deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Myhre syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Diabetes-deafness syndrome maternally transmitted |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary sensory and autonomic neuropathy with deafness and global delay |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Bartter syndrome type 4 |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Beta-D-mannosidosis |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Mutilating keratoderma |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Split-foot malformation, mesoaxial polydactyly syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
X-linked sensorineural hearing loss |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Combined oxidative phosphorylation defect type 25 |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant spastic paraplegia type 29 |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital ichthyosis, microcephalus, tetraplegia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Epibulbar lipodermoid, preauricular appendage, polythelia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Auditory neuropathy, optic atrophy syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Proliferating cell nuclear antigen-related progressive neurodegenerative photosensitivity syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Duane retraction syndrome with congenital deafness |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Otodental syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Waardenburg Shah syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Syndromic sensorineural deafness due to combined oxidative phosphorylation defect |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Epiphyseal, vertebral, ear dysplasia, nose plus associated findings syndrome |
Is a |
True |
Auditory system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|