Details of Disease

General Information of Disease (ID: DISXO7WJ)

Disease Name Premature ovarian failure 3
Synonyms Pof3; premature ovarian failure type 3; premature ovarian failure 3
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DISXO7WJ: Premature ovarian failure 3
Disease Identifiers
MONDO ID
MONDO_0012169
MESH ID
C563816
UMLS CUI
C1837008
OMIM ID
608996
MedGen ID
373230

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
FOXL2 OTFRQUYL Limited Unknown [1]
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References

1 Identification of novel mutations in FOXL2 associated with premature ovarian failure. Mol Hum Reprod. 2002 Aug;8(8):729-33. doi: 10.1093/molehr/8.8.729.