GB81 Autosomal dominant polycystic kidney disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

synonyms

• Autosomal dominant polycystic kidney disease
• adult polycystic kidney disease
• Polycystic kidney, adult type
• APCKD - [autosomal polycystic kidney disease]
• Autosomal dominant polycystic kidney disease type 1 without tuberous sclerosis
• ADPCKD1 - [autosomal dominant polycystic kidney disease type 1]
• APCKD1 - [autosomal polycystic kidney disease type 1]
• Autosomal dominant polycystic kidney disease, Type 2
• ADPCKD2 - [autosomal dominant polycystic kidney disease type 2]
• APCKD2 - [autosomal polycystic kidney disease type 2]
• PKD2 gene - [polycystic kidney disease type 2 gene]

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