Alport syndrome (Q54857): 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/1170919425 / rank | |||
Normal rank | |||
Revision as of 02:29, 14 August 2026
Alport syndrome is an inherited disease characterised by glomerular nephropathy with haematuria, progressing to end-stage renal disease, associated with sensorineural deafness and eye affection such as lenticonus or retinopathia. It involves a structural defect of type IV collagen, which is a normal component of the glomeral basal membrane.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1170919425 |
||
| English | Alport syndrome |
Alport syndrome is an inherited disease characterised by glomerular nephropathy with haematuria, progressing to end-stage renal disease, associated with sensorineural deafness and eye affection such as lenticonus or retinopathia. It involves a structural defect of type IV collagen, which is a normal component of the glomeral basal membrane. |
