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DO Term : hypogonadotropic hypogonadism 19 with or without anosmia [DOID:0090090] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the DUSP6 gene on chromosome 12q22, sometimes in association with mutations in other genes.
  • synonyms:
  • ICD10CM:E23.0,
  • 615269,
  • OMIM:615269
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Disease

Diseases --> Human genes

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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