| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hirschsprung disease with deafness and polydactyly syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Johnson neuroectodermal syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Lipodystrophy, intellectual disability, deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Severe X-linked intellectual disability Gustavson type |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Ramos Arroyo syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Nephrosis, deafness, urinary tract, digital malformation syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Caudal appendage deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Central nervous system calcification, deafness, tubular acidosis, anemia syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Coxoauricular syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Dysmorphism, short stature, deafness, disorder of sex development syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Waardenburg Shah syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Deafness with cataract and skeletal anomaly syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Wolfram-like syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Branchiootic syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Deafness, nephritis, anorectal malformation syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Hypertelorism, preauricular sinus, punctual pits, deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Wildervanck syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Auditory synaptopathy |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Hereditary hearing loss |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Progressive deafness with stapes fixation |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Deafness and oligodontia syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Melnick-Fraser syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Renal tubular acidosis with progressive nerve deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| X-linked spinocerebellar ataxia type 3 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Charcot-Marie-Tooth disease type IE |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Senter syndrome |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Keratitis ichthyosis and deafness syndrome |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal recessive keratitis-ichthyosis-deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| 3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Familial amyloid nephropathy with urticaria AND deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Albinism-deafness syndrome of Tietz |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Diabetes mellitus AND insipidus with optic atrophy AND deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Spastic paraparesis co-occurrent with deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Craniofacial deafness hand syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Emberger syndrome |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Progressive bulbar palsy with sensorineural deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Myhre syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
7 |
| Auditory dysfunction |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Diabetes-deafness syndrome maternally transmitted |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Normal auditory tuning fork test |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Hereditary sensory and autonomic neuropathy with deafness and global delay |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked hereditary sensory and autonomic neuropathy with deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Bartter syndrome type 4a |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Bartter syndrome type 4 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Tonal tinnitus |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Partial transitory deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Total transitory deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Transitory deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Neural hearing loss of right ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Neural hearing loss of left ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Conductive hearing loss of left ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Conductive hearing loss of right ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Waardenburg syndrome type 3 |
Interprets |
False |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Retinitis pigmentosa-deafness syndrome type 3 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Waardenburg syndrome type 1 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Conductive hearing loss of left ear with normal hearing on right side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Conductive hearing loss of right ear with normal hearing on left side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Sensorineural hearing loss of right ear with normal hearing on left side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Sensorineural hearing loss of left ear with normal hearing on right side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Mixed conductive and sensorineural hearing loss of right ear with normal hearing on left side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Mixed conductive and sensorineural hearing loss of left ear with normal hearing on right side |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Waardenburg syndrome type 2 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Sensorineural hearing loss of right ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Sensorineural hearing loss of left ear |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Sensorineural deafness due to late congenital syphilis |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Cardiospondylocarpofacial syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Severe X-linked intellectual disability Gustavson type |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
6 |
| Beta-D-mannosidosis |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Choroideremia with deafness and obesity syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Mutilating keratoderma |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Keratoderma hereditarium mutilans with ichthyosis syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked external auditory canal atresia, dilated internal auditory canal, facial dysmorphism syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Deafness-dystonia-optic neuronopathy syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Diaphanous related formin 1 related sensorineural hearing loss, thrombocytopenia syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Split-foot malformation, mesoaxial polydactyly syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
5 |
| Ocular albinism with late-onset sensorineural deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Mitochondrial myopathy, lactic acidosis, deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Deafness craniofacial syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Phocomelia, ectrodactyly, deafness and sinus arrhythmia syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Pili torti-deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| X-linked sensorineural hearing loss |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Combined oxidative phosphorylation defect type 25 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
1 |
| Auditory perception function |
Is a |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
|
| Maternal perinatal sensorineural hearing loss |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Neonatal sensorineural hearing loss |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Fetal sensorineural hearing loss |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal dominant spastic paraplegia type 29 |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
4 |
| Non-syndromic mitochondrial sensorineural deafness |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |
| Congenital ichthyosis, microcephalus, tetraplegia syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome |
Interprets |
True |
Hearing, function |
Inferred relationship |
Existential restriction modifier |
3 |