Disease #06909 (POF19 (ovarian failure, premature, type 19), OMIM:619245)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	POF19
Name	ovarian failure, premature, type 19
OMIM ID	619245
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HSF2BP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-07 19:04:59 +02:00 (CEST)
Date last edited	2022-04-07 19:05:31 +02:00 (CEST)

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