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| Term | primary ovarian insufficiency 18 | ID (Ontology) | DOID:0112269 (Human Disease) |
| 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. | ||
| Also Known As | "POF18" ; "premature ovarian failure 18" | ||
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autosomal genetic disease |__autosomal recessive disease____ ovarian disease | |__primary ovarian insufficiency__| primary ovarian insufficiency 18 |
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autosomal recessive disease primary ovarian insufficiency |
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| MIM:619203 | |||