Disease #06910 (SPGF70 (spermatogenic failure, type 70), OMIM:619828)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	SPGF70
Name	spermatogenic failure, type 70
OMIM ID	619828
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDHA2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-08 19:36:43 +02:00 (CEST)
Date last edited	2022-04-08 19:49:53 +02:00 (CEST)

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