Search Ontology:
Human Disease

autosomal recessive congenital bilateral absence of vas deferens

Term ID
DOID:0111864
Synonyms
Definition
A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2. https://pubmed.ncbi.nlm.nih.gov/7529962/
References
Ontology
Human Disease   ( DOID:0111864 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models