Disease #06908 (SPGF50 (spermatogenic failure, type 50), OMIM:619145)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF50
Name	spermatogenic failure, type 50
OMIM ID	619145
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	XRCC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-07 19:02:24 +02:00 (CEST)
Date last edited	N/A

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