6q25 deletion (Q97420): 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/1123604918 / rank
 
Normal rank

Revision as of 13:32, 16 August 2026

6q25 microdeletion syndrome is a chromosomal anomaly associated with developmental delay, facial dysmorphism and hearing loss.
Language Label Description Also known as
default for all languages
ID_1123604918
    English
    6q25 deletion
    6q25 microdeletion syndrome is a chromosomal anomaly associated with developmental delay, facial dysmorphism and hearing loss.

      Statements