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DO Term : hypogonadotropic hypogonadism 13 with or without anosmia [DOID:0090073] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the KISS1 gene on chromosome 1q32.

synonyms:
ICD10CM:E23.0,
614842,
OMIM:614842

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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