Disease #05563 (SPGF34 (spermatogenic failure, type 34 (SPGF-34)), OMIM:618153)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPGF34
Name	spermatogenic failure, type 34 (SPGF-34)
OMIM ID	618153
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FSIP2
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2019-02-13 22:49:41 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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