Term Name:	autosomal dominant congenital deafness with onychodystrophy
Synonyms:
Definition:	A syndrome that is characterized by autosomal dominant inheritance of congenital deafness and onychodystrophy and that has_material_basis_in heterozygous mutation in the ATP6V1B2 gene on chromosome 8p21.
Ontology:	Human Disease [DOID:0080720]   ( DOID:0080720 )