Disease #01873 (SPGF5 (spermatogenic failure, type 5 (SPGF5)), OMIM:243060)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF5
Name	spermatogenic failure, type 5 (SPGF5)
OMIM ID	243060
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AURKC
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-11-05 09:41:44 +01:00 (CET)

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