14q11.2 deletion (Q104790): 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/1854856553 / rank | |||
Normal rank | |||
Revision as of 10:39, 17 August 2026
14q11.2 microdeletion syndrome is a chromosomal anomaly syndrome characterised by developmental delay, hypotonia and facial dysmorphism (widely-spaced eyes, short nose with flat nasal bridge, long philtrum, prominent Cupid's bow, full lower lip and auricular anomalies).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1854856553 |
||
| English | 14q11.2 deletion |
14q11.2 microdeletion syndrome is a chromosomal anomaly syndrome characterised by developmental delay, hypotonia and facial dysmorphism (widely-spaced eyes, short nose with flat nasal bridge, long philtrum, prominent Cupid's bow, full lower lip and auricular anomalies). |
