Disease #05646 (SPGF28 (permatogenic failure, type 28 (SPGF-28)), OMIM:618086)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF28
Name	permatogenic failure, type 28 (SPGF-28)
OMIM ID	618086
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FANCM
Associated tissues	-
Disease features	-
Remarks	autosomal recessive
Date created	2019-08-09 12:36:41 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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