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DO Term : primary ovarian insufficiency 10 [DOID:0080867] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary ovarian insufficiency that is characterized by primary amenorrhea, hypergonadotropic ovarian insufficiency, and genomic instability in somatic cells and that has_material_basis_in homozygous mutation in the MCM8 gene on chromosome 20p.
  • synonyms:
  • 612885,
  • OMIM:612885
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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