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DO Term : hypogonadotropic hypogonadism 5 with or without anosmia [DOID:0090084] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CHD7 gene on chromosome 8q12.
  • synonyms:
  • ICD10CM:E23.0,
  • 612370,
  • OMIM:612370
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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