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DO Term : primary ovarian insufficiency 15 [DOID:0080872] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A primary ovarian insufficiency that is characterized by onset of oligomenorrhea in the third decade of life, with small ovaries, reduced number of follicles, and elevated gonadotropic hormones and that has_material_basis_in homozygous mutation in the FANCM gene on chromosome 14q21.
  • synonyms:
  • 618096,
  • OMIM:618096
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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents