Autosomal recessive Robinow syndrome (Q101943): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_793292660 | |||
| Property / CURIE: CID11:ID_793292660 / rank | |||
Normal rank | |||
Revision as of 18:47, 16 August 2026
Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_793292660 |
||
| English | Autosomal recessive Robinow syndrome |
Autosomal recessive Robinow syndrome (RRS) is the less common and the more severe type of Robinow syndrome (RS) characterised by short-limb dwarfism, costovertebral segmentation defects and abnormalities of the head, face and external genitalia. |
Statements
CID11:ID_793292660
0 references
