SYNGAP1 syndrome (Q101738): 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/1830660574 / rank
 
Normal rank

Revision as of 18:34, 16 August 2026

A neurodevelopmental encephalopathy notable for intellectual deficit with clear aetiology from a pathogenic variant of SYNGAP1.
Language Label Description Also known as
default for all languages
ID_1830660574
    English
    SYNGAP1 syndrome
    A neurodevelopmental encephalopathy notable for intellectual deficit with clear aetiology from a pathogenic variant of SYNGAP1.

      Statements