Disease #05561 (SPGF18 (spermatogenic failure, type 18 (SPGF18)), OMIM:617576)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF18
Name	spermatogenic failure, type 18 (SPGF18)
OMIM ID	617576
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DNAH1
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-02-13 21:59:39 +01:00 (CET)
Date last edited	2021-10-22 15:37:15 +02:00 (CEST)

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