Dentinogenesis imperfecta type 2 (Q86046): Difference between revisions
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13 August 2026
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Latest revision as of 11:24, 15 August 2026
Type 2 occurs in people without other inherited disorders (i.e. Osteogenesis imperfecta), it is an autosomal dominant trait, while a few families with type II have progressive hearing loss in addition to dental abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_314718507 |
||
| English | Dentinogenesis imperfecta type 2 |
Type 2 occurs in people without other inherited disorders (i.e. Osteogenesis imperfecta), it is an autosomal dominant trait, while a few families with type II have progressive hearing loss in addition to dental abnormalities. |
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CID11:ID_314718507
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dki-india-ID_314718507
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Concluído
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13 August 2026
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