Disease association ontology term - MONDO:0030058 - hearing loss, autosomal dominant 77
Term summary
ID
MONDO:0030058
Name
hearing loss, autosomal dominant 77
Ontology or CV name
Disease association
Parents
is_a
autosomal dominant nonsyndromic hearing loss
Annotation
Disease association
MONDO:0030058
-
hearing loss, autosomal dominant 77
References:
PB_REF:0000006
Genes:
abc1 (SPAC9E9.12c)
abc2 (SPAC3F10.11c)
abc3 (SPBC359.05)
abc4 (SPAC30.04c)