Uniparental disomies of paternal origin (Q46779): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / 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 the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD45.1 |
||
| English | Uniparental disomies of paternal origin |
Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing. |
Statements
CID11:LD45.1
0 references
dki-india-LD45.1
0 references
Concluído
0 references
