Details of Disease

General Information of Disease (ID: DISN1FHW)

Disease Name Premature ovarian failure 21
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DISN1FHW: Premature ovarian failure 21
Disease Identifiers
MONDO ID
MONDO_0957216
UMLS CUI
C5830399
OMIM ID
620311
MedGen ID
1841035

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
TP63 OT0WOOKQ Strong Autosomal dominant [1]
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References

1 TP63-truncating variants cause isolated premature ovarian insufficiency. Hum Mutat. 2019 Jul;40(7):886-892. doi: 10.1002/humu.23744. Epub 2019 Mar 29.