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What (who) is cystic disease - definition

INHERITED FORM OF CYSTIC KIDNEY DISEASE LEADING TO FIBROSIS AND IMPAIRED RENAL FUNCTION THAT IS CAUSED BY MUTATIONS IN THE UMOD GENE, WHICH ENCODES UROMODULIN/TAMM-HORSFALL MUCOPROTEIN

Medullary cystic disease; Medullary cystic renal disease; Autosomal-dominant medullary cystic kidney disease

Cystic kidney disease

CONGENITAL OR ACQUIRED KIDNEY DISORDER CHARACTERIZED BY THE PRESENCE OF RENAL CYSTS

Cystic kidney diseases; Kidney diseases, cystic

Cystic kidney disease refers to a wide range of hereditary, developmental, and acquired conditions and with the inclusion of neoplasms with cystic changes, over 40 classifications and subtypes have been identified. Depending on the disease classification, the presentation may be at birth, or much later into adult life.

https://en.wikipedia.org/wiki/Cystic_kidney_disease

cystic fibrosis

AUTOSOMAL RECESSIVE DISEASE CHARACTERIZED BY THE BUILDUP OF MUCUS

Mucoviscidosis; Cistic fibrosis; Cystic Fiborsis; Cystic fibrosis allele; Cystic fibrose; Mucoviscidose; Viscoidosis; Mucuviscoidosis; Mucoviscoidosis; Mucoviscidopsis; Fibrocystic disease of the pancreas; Cystic Fibrosis; Cyctic fibrosis; Cystic Fibrosis (CF); History of Cystic fibrosis; Gene therapy for cystic fibrosis; Treatment of cystic fibrosis

Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult.

N-UNCOUNT

Polycystic liver disease

HUMAN DISEASE

Polycystic Liver Disease; Cystic disease of liver

Polycystic liver disease (PLD) usually describes the presence of multiple cysts scattered throughout normal liver tissue. PLD is commonly seen in association with autosomal-dominant polycystic kidney disease, with a prevalence of 1 in 400 to 1000, and accounts for 8–10% of all cases of end-stage renal disease.

https://en.wikipedia.org/wiki/Polycystic_liver_disease

Wikipedia

Medullary cystic kidney disease

Medullary cystic kidney disease (MCKD) is an autosomal dominant kidney disorder characterized by tubulointerstitial sclerosis leading to end-stage renal disease. Because the presence of cysts is neither an early nor a typical diagnostic feature of the disease, and because at least 4 different gene mutations may give rise to the condition, the name autosomal dominant tubulointerstitial kidney disease (ADTKD) has been proposed, to be appended with the underlying genetic variant for a particular individual. Importantly, if cysts are found in the medullary collecting ducts they can result in a shrunken kidney, unlike that of polycystic kidney disease. There are two known forms of medullary cystic kidney disease, mucin-1 kidney disease 1 (MKD1) and mucin-2 kidney disease/uromodulin kidney disease (MKD2). A third form of the disease occurs due to mutations in the gene encoding renin (ADTKD-REN), and has formerly been known as familial juvenile hyperuricemic nephropathy type 2.

https://en.wikipedia.org/wiki/Medullary cystic kidney disease