Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bartter syndrome type 4a (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
4 |
Bartter syndrome type 4 |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Partial transitory deafness (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
3 |
Total transitory deafness |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
3 |
Transitory deafness |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
3 |
Neural hearing loss of right ear |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Neural hearing loss of left ear (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Retinitis pigmentosa-deafness syndrome type 3 (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
1 |
Sensorineural deafness due to late congenital syphilis |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
1 |
Beta-D-mannosidosis |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
1 |
Mutilating keratoderma |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
5 |
Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
3 |
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
5 |
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
5 |
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
4 |
Split-foot malformation, mesoaxial polydactyly syndrome |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
4 |
Ocular albinism with late-onset sensorineural deafness (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Congenital hearing disorder |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
1 |
Deafness craniofacial syndrome (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
7 |
Pili torti-deafness syndrome |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
3 |
X-linked sensorineural hearing loss |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |
Combined oxidative phosphorylation defect type 25 (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
4 |
Autosomal dominant spastic paraplegia type 29 (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
5 |
Non-syndromic mitochondrial sensorineural deafness (disorder) |
Finding site |
True |
Structure of auditory system (body structure) |
Inferred relationship |
Some |
2 |