DEAFNESS, AUTOSOMAL RECESSIVE 20

General Information (adopted from Orphanet):

Synonyms, Signs: DFNB20
Number of Symptoms 1
OrphanetNr:
OMIM Id: 604060
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0000365) Hearing impairment 539 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Clinical Description OMIM Moynihan et al. (1999) studied a family in which hearing impairment was diagnosed between the ages of 3 months and 1 year.