Weissenbacher- Zweymuller syndrome (Q88326): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 14:31, 15 August 2026
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1421501711 |
||
| English | Weissenbacher- Zweymuller syndrome |
Weissenbacher-Zweymuller syndrome is a genetic disorder characterised by short stature at birth, neonatal micrognathia, cleft palate, rhizomelic chondrodysplasia with 'dumbbell' shaped arm and leg bones, hypertelorism and vertebral coronal clefts. |
Statements
CID11:ID_1421501711
0 references
dki-india-ID_1421501711
0 references
Concluído
0 references
13 August 2026
0 references
