Brachyolmia type 3 (Q101702): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A braquiolmia tipo 3 é uma forma de braquiolmia autossômica dominante, moderadamente grave, um grupo de transtornos esqueléticos genéticos raros, e que é caracterizada por baixa estatura, platiespondilia e cifoescoliose grave. | |||
| description / en | description / en | ||
Brachyolmia type 3 is an autosomal dominant, mildly severe form of brachyolmia, a group of rare genetic skeletal disorders, and is characterised by short stature, platyspondyly and severe kyphoscoliosis. | |||
Revision as of 18:32, 16 August 2026
Brachyolmia type 3 is an autosomal dominant, mildly severe form of brachyolmia, a group of rare genetic skeletal disorders, and is characterised by short stature, platyspondyly and severe kyphoscoliosis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_589025803 |
||
| English | Brachyolmia type 3 |
Brachyolmia type 3 is an autosomal dominant, mildly severe form of brachyolmia, a group of rare genetic skeletal disorders, and is characterised by short stature, platyspondyly and severe kyphoscoliosis. |
