Disease #06914 (SPGF66 (spermatogenic failure, type 66), OMIM:619799)

Global Variome shared LOVD

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

Official abbreviation	SPGF66
Name	spermatogenic failure, type 66
OMIM ID	619799
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ZPBP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-09 21:06:35 +02:00 (CEST)
Date last edited	N/A

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