| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |
| Autosomal dominant deafness with onychodystrophy syndrome |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |
| Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |
| Auditory neuropathy, optic atrophy syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| PCNA-related progressive neurodegenerative photosensitivity syndrome |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Duane retraction syndrome with congenital deafness |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Profound hearing loss |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
1 |
| Congenital cochleovestibular malformation |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Otodental syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Progressive autosomal recessive cerebellar ataxia, sensorineural hearing loss syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
1 |
| Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Waardenburg syndrome type 3 (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Senter syndrome |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Keratitis ichthyosis and deafness syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Juvenile-onset diabetes mellitus, central and peripheral neurodegeneration syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |
| Syndromic sensorineural deafness due to combined oxidative phosphorylation defect |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Non-syndromic genetic hearing loss |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
1 |
| Postlingual non-syndromic genetic deafness |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
1 |
| Prelingual non-syndromic genetic deafness (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
1 |
| Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Subjective pulsatile tinnitus |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Bilateral subjective pulsatile tinnitus of ears |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Subjective pulsatile tinnitus of left ear |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Subjective pulsatile tinnitus of right ear (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| High frequency sensorineural hearing loss (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| High frequency conductive hearing loss (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Mondini defect (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Low frequency sensorineural hearing loss |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Low frequency conductive hearing loss (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
2 |
| Usher syndrome type 1F (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
4 |
| Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
6 |
| Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
6 |
| Wolfram syndrome type 1 (disorder) |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |
| Wolfram syndrome type 2 |
Interprets |
True |
Hearing |
Inferred relationship |
Some |
3 |