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 -

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