Oculocerebral syndrome with hypopigmentation (Q90678): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 17:39, 15 August 2026
Rare syndrome characterised by hypopigmentation of the skin, microphthalmia and cerebral abnormalities which result in spasticity and mental retardation.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1046083935 |
||
| English | Oculocerebral syndrome with hypopigmentation |
Rare syndrome characterised by hypopigmentation of the skin, microphthalmia and cerebral abnormalities which result in spasticity and mental retardation. |
Statements
CID11:ID_1046083935
0 references
dki-india-ID_1046083935
0 references
Concluído
0 references
13 August 2026
0 references
