Disease #07134 (SPGF96 (spermatogenic failure, type 96), OMIM:621001)

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	SPGF96
Name	spermatogenic failure, type 96
OMIM ID	621001
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SPATA22
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-11-24 14:03:42 +01:00 (CET)
Date last edited	N/A

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