Deafness, sensorineural, variable

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Sensorineural deafness, variable (in 1 family) [OMIM:Sensorineural deafness, variable (in 1 family)]
Quality:
Cross references:
OMIM: "Deafness, sensorineural, variable" [OMIM:Deafness, sensorineural, variable]
OMIM: "Sensorineural deafness, variable (in 1 family)" [OMIM:Sensorineural deafness, variable (in 1 family)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2N (Orphanet:228174)
Nonacquired combined pituitary hormone deficiency with spine abnormalities (Orphanet:231720)