Ophthalmoacromelic syndrome (Q94956): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
Microftalmia com anomalias de membros, também conhecida como síndrome oftalmo-acromélica, é um transtorno do desenvolvimento raro caracterizado por microftalmia ou anoftalmia bilateral, sinostose, sindactilia, oligodactilia e/ou polidactilia. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/1788103611 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_1788103611 | |||||||||||||||
| Property / CURIE: CID11:ID_1788103611 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_1788103611 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1788103611 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 10:31, 16 August 2026
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1788103611 |
||
| English | Ophthalmoacromelic syndrome |
Microphthalmia with limb anomalies, also known as ophthalmo-acromelic syndrome, is a rare developmental disorder characterised by bilateral microphthalmia or anophthalmia, synostosis, syndactyly, oligodactyly and/or polydactyly. |
Statements
CID11:ID_1788103611
0 references
dki-india-ID_1788103611
0 references
Concluído
0 references
15 August 2026
0 references
