Disease association ontology term - MONDO:0032639 - hearing loss, autosomal recessive 112

Term summary

ID: MONDO:0032639
Name: hearing loss, autosomal recessive 112
Ontology or CV name: Disease association

Parents

is_a hearing loss, autosomal recessive

Annotation

Disease association

MONDO:0032639 - hearing loss, autosomal recessive 112

References:

PB_REF:0000006

Genes:

bdp1 (SPCC1919.14c)