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

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	CBAVD
Name	vas deferens, congenital bilateral absence (CBAVD)
OMIM ID	277180
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	1
Associated with 1 gene	CFTR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-05-14 09:31:10 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.