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 |
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