OBO ID: DOID:0080859
Term Name: primary ovarian insufficiency 2B Search Ontology:
Synonyms:
Definition: A primary ovarian insufficiency that has_material_basis_in mutation in the POF1B gene. https://pubmed.ncbi.nlm.nih.gov/16773570/
References:
Ontology: Human Disease   ( DOID:0080859 )
Relationships
is a type of:
OTHER primary ovarian insufficiency 2B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
POF1B ?Premature ovarian failure 2B 300604
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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