Structured Summary
Abstract
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.
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Classification
Broader headings
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MeSH Record
Synonyms
9 entry terms
- ARPKD
- Autosomal Recessive Polycystic Kidney Disease
- Kidney, Polycystic, Autosomal Recessive
- Polycystic Kidney Disease, Autosomal Recessive
- Polycystic Kidney Disease, Infantile, Type 1
- Polycystic Kidney Disease, Infantile, Type I
- Polycystic Kidney and Hepatic Disease 1
- Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
- Polycystic Kidney, Autosomal Recessive
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
1992
MeSH Record
Previous Indexing
- Kidney, Polycystic (1966-1991)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Autosomal Recessive Polycystic Kidney. Medical Subject Headings (MeSH). 2026. Unique ID D017044. http://id.nlm.nih.gov/mesh/2026/D017044
- Autosomal Recessive Polycystic Kidney. In: Wikipedia. https://en.wikipedia.org/wiki/Autosomal_recessive_polycystic_kidney_disease
- Autosomal Recessive Polycystic Kidney. In: Wikidata. https://www.wikidata.org/wiki/Q3395618