Autosomal dominant polycystic kidney disease

ICD-11 code : GB81;

Preferred Label : Autosomal dominant polycystic kidney disease;

ICD-11 definition : Multiple cysts in both kidneys increasing in number and size from adolescence, associated with development of hypertension and chronic renal failure. Autosomal dominant familial pattern is usual and due to mutations on Chromosomes 16 and 4. Non-renal manifestations can include cysts in the liver and less commonly pancreas,. Cerebral arterial aneurysms with subarachnoid haemorrhage, and other non-renal vascular abnormalities can also occur.;

ICD-11 synonym : APCKD - [autosomal polycystic kidney disease]; adult polycystic kidney disease; Polycystic kidney, adult type; autosomal polycystic kidney disease;

ICD-11 acronym : APCKD;

Détails

Origin ID

91220434;

Currated CISMeF NLP mapping
- Autosomal Dominant Polycystic Kidney Disease [NCIt concept]
- Autosomal dominant polycystic kidney disease [ORDO Disease]
- Autosomal dominant polycystic kidney disease (disorder) [SNOMED CT concept]
- Polycystic kidney disease 1 with or without polycystic liver disease [OMIM Phenotype]
- Polycystic kidney disease, adult type (disorder) [Inactive SNOMED CT concept]
- Polycystic kidney, adult type [ICD-10 Sub-category]
- Polycystic kidney, adult type [ICD-10 Sub-category (who)]
- Polycystic kidney, autosomal dominant [ICD-9 code]
- Polycystic kidney, autosomal dominant [MedDRA LLT]
- autosomal dominant polycystic kidney disease [DO Concept]
- autosomal dominant polycystic kidney disease [Disease (Nov.)]
- polycystic kidney, autosomal dominant [MeSH concept]
- polycystic kidney, autosomal dominant [MeSH Descriptor]
ICD-10 Mapping
- Polycystic kidney, adult type [ICD-10 Sub-category]

Position du mot-clé dans l'(les) arborescence(s) :

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