Deafness – onychodystrophy, autosomal recessive (Q98468): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
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 |
|---|---|---|---|
| default for all languages | ID_1781537287 |
||
| 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
0 references
dki-india-ID_1781537287
0 references
Concluído
0 references
15 August 2026
0 references
