Disease #06919 (SPGF62 (spermatogenic failure, type 62), OMIM:619673)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: David Baux

Official abbreviation	SPGF62
Name	spermatogenic failure, type 62
OMIM ID	619673
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RNF212
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-13 11:44:54 +02:00 (CEST)
Date last edited	N/A

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