Dyggve-Melchior-Clausen disease (Q88337): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_21266164 | |||
| Property / CURIE: CID11:ID_21266164 / rank | |||
Normal rank | |||
Revision as of 14:32, 15 August 2026
Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_21266164 |
||
| English | Dyggve-Melchior-Clausen disease |
Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity. |
Statements
CID11:ID_21266164
0 references
