Disease #06913 (SPGF68 (spermatogenic failure, type 68), OMIM:619805)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF68
Name	spermatogenic failure, type 68
OMIM ID	619805
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ALS2CR11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-09 21:05:07 +02:00 (CEST)
Date last edited	N/A

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