Preferred Name

Dentinogenesis Imperfecta [Disease/Finding]
Synonyms

Dentinogenesis Imperfecta

ID

http://purl.bioontology.org/ontology/NDFRT/N0000000935

altLabel

Dentinogenesis Imperfecta

cui

C0011436

MESH DEFINITION

An autosomal dominant disorder of tooth development characterized by opalescent dentin resulting in discoloration of the teeth. The dentin develops poorly with low mineral content while the pulp canal is obliterated.

MESH DUI

D003811

MeSH name

Dentinogenesis Imperfecta

MESH UI

M0005958

NDFRT kind

DISEASE_KIND

notation

N0000000935

NUI

N0000000935

prefLabel

Dentinogenesis Imperfecta [Disease/Finding]

SNOMED CID

196286005

tui

T019

subClassOf

http://purl.bioontology.org/ontology/NDFRT/N0000002970

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