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. | |||||||||||||||
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Deafness Onychodystrophy Onycholysis Retardation (DOOR) syndrome is characterised by sensorineural hearing loss, distinctive nail abnormalities and bone malformations, and mild to profound mental retardation. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1781537287 / rank | |||||||||||||||
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CID11:ID_1781537287 | |||||||||||||||
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dki-india-ID_1781537287 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest 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 |
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| 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. |
Statements
CID11:ID_1781537287
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dki-india-ID_1781537287
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Concluído
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15 August 2026
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