Ectodermal dysplasia syndromes (Q46654): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-LD27.0 | |||
| Property / Canary Token: dki-india-LD27.0 / rank | |||
Normal rank | |||
Revision as of 15:23, 13 August 2026
Ectodermal dysplasias (EDs) are a heterogeneous group of syndromes characterised by developmental dystrophies of ectodermal structures, such as hypohidrosis, hypotrichosis, onychodysplasia and hypodontia or anodontia. More than 160 clinically and genetically distinct hereditary ectodermal dysplasia syndromes have been catalogued.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD27.0 |
||
| English | Ectodermal dysplasia syndromes |
Ectodermal dysplasias (EDs) are a heterogeneous group of syndromes characterised by developmental dystrophies of ectodermal structures, such as hypohidrosis, hypotrichosis, onychodysplasia and hypodontia or anodontia. More than 160 clinically and genetically distinct hereditary ectodermal dysplasia syndromes have been catalogued. |
Statements
CID11:LD27.0
0 references
dki-india-LD27.0
0 references
