Disease #05567 (SPGF19 (spermatogenic failure, type 19 (SPGF-19)), OMIM:617592)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF19
Name	spermatogenic failure, type 19 (SPGF-19)
OMIM ID	617592
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	WDR96
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-02-13 22:57:31 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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