OBO ID: DOID:0111526 |
Term Name: | Mullerian aplasia and hyperandrogenism | Search Ontology: | |
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Definition: | A disorder of sexual development characterized by primary amenorrhea, an underdeveloped or absent uterus, and clinical hyperandrogenism that has_material_basis_in heterozygous mutation in the WNT4 gene on chromosome 1p36.12. https://www.ncbi.nlm.nih.gov/pubmed/15317892 | ||
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Ontology: | Human Disease ( DOID:0111526 ) |
OTHER Mullerian aplasia and hyperandrogenism PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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