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DO Term : hypogonadotropic hypogonadism 22 with or without anosmia [DOID:0090081] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the FEZF1 gene on chromosome 7q31.

synonyms:
ICD10CM:E23.0,
OMIM:616030,
616030

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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