ZFIN Human Disease: autosomal recessive congenital bilateral absence of vas deferens

OBO ID: DOID:0111864

Term Name:	autosomal recessive congenital bilateral absence of vas deferens		Search Ontology:
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:	OMIM:277180
Ontology:	Human Disease ( DOID:0111864 )

Relationships

is a type of:	autosomal recessive disease congenital bilateral absence of vas deferens autosomal recessive disease congenital bilateral absence of vas deferens Show first 5 Terms

OTHER autosomal recessive congenital bilateral absence of vas deferens PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CFTR	cftr	Congenital bilateral absence of vas deferens	277180

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None