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DO Term : primary ovarian insufficiency 19 [DOID:0112278] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary ovarian insufficiency characterized by irregular menses that cease in the third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the HSF2BP gene on chromosome 21q22.
  • synonyms:
  • premature ovarian failure 19,
  • POF19,
  • POI19,
  • 619245,
  • OMIM:619245
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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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