Disease #06898 (POF18 (ovarian failure, premature, type 18), OMIM:619203)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	POF18
Name	ovarian failure, premature, type 18
OMIM ID	619203
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C14orf39
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-02-16 19:57:14 +01:00 (CET)
Date last edited	N/A

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