Details of Disease

General Information of Disease (ID: DIS17J15)

Disease Name Premature ovarian failure 13
Synonyms POF13; premature ovarian failure 13
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DIS17J15: Premature ovarian failure 13
Disease Identifiers
MONDO ID
MONDO_0044317
UMLS CUI
C4479510
OMIM ID
617442
MedGen ID
1393321

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
MSH5 OTDARQT3 Limited Unknown [1]
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References

1 Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease. Gastroenterology. 2015 Nov;149(6):1415-24. doi: 10.1053/j.gastro.2015.07.006. Epub 2015 Jul 17.