OBO ID: DOID:0080859 |
Term Name: | primary ovarian insufficiency 2B | Search Ontology: | |
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Definition: | A primary ovarian insufficiency that has_material_basis_in mutation in the POF1B gene. https://pubmed.ncbi.nlm.nih.gov/16773570/ | ||
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Ontology: | Human Disease ( DOID:0080859 ) |
OTHER primary ovarian insufficiency 2B PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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