Disease #00131 (CBAVD (vas deferens, congenital bilateral absence (CBAVD)), OMIM:277180)

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	Curator: Johan T. den Dunnen

Official abbreviation	CBAVD
Name	vas deferens, congenital bilateral absence (CBAVD)
OMIM ID	277180
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CFTR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-05-14 09:31:10 +02:00 (CEST)
Date last edited	N/A