Disease #06940 (SPGFX3 (spermatogenic failure, X-linked, type 3), OMIM:301059)

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	SPGFX3
Name	spermatogenic failure, X-linked, type 3
OMIM ID	301059
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CXorf59
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-06-06 22:14:00 +02:00 (CEST)
Date last edited	N/A

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