Disease #05857 (SPGF32 (spermatogenic failure, type 32 (SPGF32)), OMIM:618115)

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	SPGF32
Name	spermatogenic failure, type 32 (SPGF32)
OMIM ID	618115
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SOHLH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-19 11:13:34 +02:00 (CEST)
Date last edited	N/A

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