Disease #05456 (RPRGL1 (pregnancy loss, recurrent, susceptibility to, type 1 (RPRGL-1)), OMIM:614389)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RPRGL1
Name	pregnancy loss, recurrent, susceptibility to, type 1 (RPRGL-1)
OMIM ID	614389
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	F5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2018-07-11 09:01:11 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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