Dyggve-Melchior-Clausen disease (Q88337): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Changed label, description and/or aliases in pt-br, en
‎Changed an Item
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/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