Dentinogenesis imperfecta type 2 (Q86046): Difference between revisions
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O tipo 2 ocorre em pessoas sem outros transtornos hereditários (ou seja, Osteogênese imperfeita); é um traço autossômico dominante, enquanto algumas famílias com tipo II têm perda auditiva progressiva somada às anomalias dentárias. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
