Disease #03040 (POF5 (ovarian failure, premature, type 5 (POF5)), OMIM:611548)

Official abbreviation POF5
Name ovarian failure, premature, type 5 (POF5)
OMIM ID 611548
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NOBOX
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-12-01 17:15:41 +01:00 (CET)


Individuals

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00402737 - - - F no Belgium Italy - - - - POF5 premature ovarian insufficiency; 20y-hypergonadotrophic hypogonadism, secondary amenorrhea NOBOX NOBOX 1 1 Asma Sassi
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