15q24 deletion (Q101705): 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/1382727392 / rank | |||
Normal rank | |||
Revision as of 18:32, 16 August 2026
15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1382727392 |
||
| English | 15q24 deletion |
15q24 microdeletion syndrome is a rare, recently described syndrome characterised cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies. |
