Disease #05800 (SPGF1 (spermatogenic failure, type 1 (SPGF1)), OMIM:258150)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF1
Name	spermatogenic failure, type 1 (SPGF1)
OMIM ID	258150
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SYCP2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-07-26 16:53:18 +02:00 (CEST)
Date last edited	N/A

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