Disease #06897 (SPGF52 (spermatogenic failure, type 52), OMIM:619202)

Global Variome shared LOVD

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

Official abbreviation	SPGF52
Name	spermatogenic failure, type 52
OMIM ID	619202
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C14orf39
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-02-16 19:55:44 +01:00 (CET)
Date last edited	N/A

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