Disease #06931 (SPGF48 (spermatogenic failure, type 48), OMIM:619108)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF48
Name	spermatogenic failure, type 48
OMIM ID	619108
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	M1AP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-14 21:14:59 +02:00 (CEST)
Date last edited	N/A

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