Disease #06920 (SPGF61 (spermatogenic failure, type 61), OMIM:619672)

Global Variome shared LOVD

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

	Curator: Cynthia Silveira

Official abbreviation	SPGF61
Name	spermatogenic failure, type 61
OMIM ID	619672
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	STAG3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-13 11:47:47 +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.