Polycystic Kidney, Autosomal Recessive
A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY.
Year introduced: 1992
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Subheadings:
Tree Number(s): C12.050.351.968.419.403.875.510, C12.200.777.419.403.875.510, C12.950.419.403.875.510, C16.131.077.717.510, C16.320.184.625.510
MeSH Unique ID: D017044
Entry Terms:
- Autosomal Recessive Polycystic Kidney
- Kidney, Polycystic, Autosomal Recessive
- Autosomal Recessive Polycystic Kidney Disease
- ARPKD
- Polycystic Kidney Disease, Infantile, Type I
- Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
- Polycystic Kidney Disease, Autosomal Recessive
- Polycystic Kidney Disease, Infantile, Type 1
- Polycystic Kidney and Hepatic Disease 1
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