Disease association ontology term - MONDO:0010799 - deafness, aminoglycoside-induced
Term summary
ID
MONDO:0010799
Name
deafness, aminoglycoside-induced
Ontology or CV name
Disease association
Parents
is_a
postlingual non-syndromic genetic hearing loss
is_a
mitochondrial oxidative phosphorylation disorder
Annotation
Disease association
MONDO:0010799
-
deafness, aminoglycoside-induced
References:
PB_REF:0000006
Genes:
slm3 (SPAC23H4.04)