Details of Disease

General Information of Disease (ID: DISVLGB3)

Disease Name Premature ovarian failure 16
Synonyms POF16; PREMATURE OVARIAN FAILURE 16
Disease Hierarchy
DIS4V9SY: Inherited primary ovarian failure
DISVLGB3: Premature ovarian failure 16
Disease Identifiers
MONDO ID
MONDO_0032881
UMLS CUI
C5231474
OMIM ID
618723
MedGen ID
1684679

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
BNC1 OTGJ5WUF Limited Unknown [1]
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References

1 De novo copy number variants are associated with congenital diaphragmatic hernia. J Med Genet. 2012 Oct;49(10):650-9. doi: 10.1136/jmedgenet-2012-101135.