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DO Term : hypogonadotropic hypogonadism 12 with or without anosmia [DOID:0090072] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21.
  • synonyms:
  • familial hypogonadotrophic eunuchoidism,
  • familial idiopathic gonadotrpin deficiency,
  • OMIM:614841,
  • 614841,
  • ICD10CM:E23.0
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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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