OBO ID: DOID:0080869 |
Term Name: | primary ovarian insufficiency 12 | Search Ontology: | |
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Synonyms: |
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Definition: | A primary ovarian insufficiency that has_material_basis_in homozygous mutation in the SYCE1 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/25062452/ | ||
References: | |||
Ontology: | Human Disease ( DOID:0080869 ) |
OTHER primary ovarian insufficiency 12 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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SYCE1 | ?Premature ovarian failure 12 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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