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DO Term : hypogonadotropic hypogonadism 20 with or without anosmia [DOID:0090082] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes.
  • synonyms:
  • 615270,
  • ICD10CM:E23.0,
  • OMIM:615270
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