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DO Term : amelogenesis imperfecta hypomaturation type 2A5 [DOID:0110063] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An amelogenesis imperfecta that has_material_basis_in homozygous mutation in the SLC24A4 gene on chromosome 14q32.

synonyms:
amelogenesis imperfecta hypomaturation type IIA5,
ICD10CM:K00.5,
615887,
amelogenesis imperfecta type IIA5,
OMIM:615887,
AI2A5

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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