Disease #04437 (DFNB66 (deafness?, autosomal recessive, type 66 (DFNB-66)), OMIM:610212)

Official abbreviation DFNB66
Name deafness?, autosomal recessive, type 66 (DFNB-66)
OMIM ID 610212
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DCDC2
Associated tissues -
Disease features -
Remarks -