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loading...| Preferred Name |
Amelogenesis Imperfecta [Disease/Finding] |
|
| Synonyms |
Amelogenesis Imperfecta |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000000367 |
|
| altLabel |
Amelogenesis Imperfecta Congenital Enamel Hypoplasia |
|
| cui |
C0002452 |
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| MESH DEFINITION |
A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION. |
|
| MESH DUI |
D000567 |
|
| MeSH name |
Amelogenesis Imperfecta |
|
| MESH UI |
M0000886 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000000367 |
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| NUI |
N0000000367 |
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| prefLabel |
Amelogenesis Imperfecta [Disease/Finding] |
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| SNOMED CID |
78494001 |
|
| tui |
T019 |
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| subClassOf |
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