Details of Disease

General Information of Disease (ID: DISEPD0O)

Disease Name Premature ovarian failure 17
Synonyms POF17; premature ovarian failure 17
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DISEPD0O: Premature ovarian failure 17
Disease Identifiers
MONDO ID
MONDO_0030870
UMLS CUI
C5436889
OMIM ID
619146
MedGen ID
1748767

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
XRCC2 OTJB2PV4 Limited Unknown [1]
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References

1 XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans. Clin Genet. 2019 Mar;95(3):442-443. doi: 10.1111/cge.13475. Epub 2018 Nov 29.