Bardet-Biedl syndrome (Q94128): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_255526264 | |||
| Property / Canary Token: dki-india-ID_255526264 / rank | |||
Normal rank | |||
Revision as of 09:14, 16 August 2026
Bardet-Biedl syndrome is a ciliopathy with multisystem involvement that is characterised by a combination of clinical signs: obesity, pigmentary retinopathy, post-axial polydactyly, polycystic kidneys, hypogenitalism, and learning disabilities, many of which appear several years after disease onset.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_255526264 |
||
| English | Bardet-Biedl syndrome |
Bardet-Biedl syndrome is a ciliopathy with multisystem involvement that is characterised by a combination of clinical signs: obesity, pigmentary retinopathy, post-axial polydactyly, polycystic kidneys, hypogenitalism, and learning disabilities, many of which appear several years after disease onset. |
Statements
CID11:ID_255526264
0 references
dki-india-ID_255526264
0 references
