Deafness – onychodystrophy, autosomal recessive (Q98468): Difference between revisions
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Síndrome de surdez, onicodistrofia, onicólise e desenvolvimento intelectual comprometido (síndrome DOOR) é caracterizada por perda auditiva neurossensorial, anormalidades distintas nas unhas, malformações ósseas e retardo mental de leve a grave. | |||
| description / en | description / en | ||
Deafness Onychodystrophy Onycholysis Retardation (DOOR) syndrome is characterised by sensorineural hearing loss, distinctive nail abnormalities and bone malformations, and mild to profound mental retardation. | |||
Revision as of 14:57, 16 August 2026
Deafness Onychodystrophy Onycholysis Retardation (DOOR) syndrome is characterised by sensorineural hearing loss, distinctive nail abnormalities and bone malformations, and mild to profound mental retardation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1781537287 |
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| English | Deafness – onychodystrophy, autosomal recessive |
Deafness Onychodystrophy Onycholysis Retardation (DOOR) syndrome is characterised by sensorineural hearing loss, distinctive nail abnormalities and bone malformations, and mild to profound mental retardation. |
