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DO Term : hypogonadotropic hypogonadism 24 without anosmia [DOID:0090088] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14.
  • synonyms:
  • ORDO:52901,
  • OMIM:229070,
  • 229070,
  • ICD10CM:E23.6,
  • isolated follicle-stimulating hormone deficiency
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Disease

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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct parents





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