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DO Term : dentinogenesis imperfecta [DOID:4154] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A tooth disease characterized by discolored, opalescent teeth that has_material_basis_in mutation in the DSPP gene on chromosome 4q22.

synonyms:
OMIM:125500,
SNOMEDCT_US_2023_03_01:367461002,
125490,
ORDO:49042,
OMIM:125490,
MESH:D003811,
GARD:6258,
UMLS_CUI:C0011436,
NCI:C84667,
ICD10CM:K00.5,
125500

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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