Disease #05651 (SPGF17 (spermatogenic failure, type 17 (SPGF-17)), OMIM:617214)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF17
Name	spermatogenic failure, type 17 (SPGF-17)
OMIM ID	617214
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PLCZ1
Associated tissues	-
Disease features	-
Remarks	autosomal recessive
Date created	2019-09-13 10:35:38 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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