Details of Disease

General Information of Disease (ID: DISJGHV0)

Disease Name Premature ovarian failure 9
Synonyms Pof9; primary ovarian failure caused by mutation in HFM1; premature ovarian failure type 9; premature ovarian failure 9; HFM1 primary ovarian failure
Definition Any primary ovarian failure in which the cause of the disease is a mutation in the HFM1 gene.
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DISJGHV0: Premature ovarian failure 9
Disease Identifiers
MONDO ID
MONDO_0014322
UMLS CUI
C3810376
OMIM ID
615724
MedGen ID
816706

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
HFM1 OTHV3EFE Limited Unknown [1]
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References

1 Mutations in HFM1 in recessive primary ovarian insufficiency. N Engl J Med. 2014 Mar 6;370(10):972-4. doi: 10.1056/NEJMc1310150.