Disease #05030 (SPGFX2 (spermatogenic failure, X-linked, type 2), OMIM:309120)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGFX2
Name	spermatogenic failure, X-linked, type 2
OMIM ID	309120
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TEX11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	2022-08-19 18:32:18 +02:00 (CEST)

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