Disease #00078 (CBAVD (VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF), OMIM:277180)

Official abbreviation CBAVD
Name VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF
OMIM ID 277180
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CFTR
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 08:58:33 +00:00 (UTC)
Date last edited N/A