OBO ID: DOID:0112269 |
Term Name: | primary ovarian insufficiency 18 | Search Ontology: | |
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Synonyms: |
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Definition: | A primary ovarian insufficiency characterized by irregular menstrual cycles and cessation of menstruation in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in C14orf39 on chromosome 14q23.1. https://pubmed.ncbi.nlm.nih.gov/33508233/ | ||
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Ontology: | Human Disease ( DOID:0112269 ) |
OTHER primary ovarian insufficiency 18 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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C14orf39 | ?Premature ovarian failure 18 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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