Disease #06912 (SPGF67 (spermatogenic failure, type 67), OMIM:619803)

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	SPGF67
Name	spermatogenic failure, type 67
OMIM ID	619803
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CCDC62
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-08 20:44:34 +02:00 (CEST)
Date last edited	2022-04-09 21:05:02 +02:00 (CEST)

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