Uniparental disomies (Q46785): 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/694223526 / rank | |||
Normal rank | |||
Revision as of 15:35, 13 August 2026
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD45 |
||
| English | Uniparental disomies |
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing. |
