Concept information
Preferred term
Polycystic Kidney, Autosomal Recessive
Type
-
Topical Descriptor
Broader concept
Entry terms
- ARPKD
- Autosomal Recessive Polycystic Kidney
- Autosomal Recessive Polycystic Kidney Disease
- Kidney, Polycystic, Autosomal Recessive
- Polycystic Kidney and Hepatic Disease 1
- Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive)
- Polycystic Kidney Disease, Autosomal Recessive
- Polycystic Kidney Disease, Infantile, Type 1
- Polycystic Kidney Disease, Infantile, Type I
Scope note
- 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.
History note
- 1992
In other languages
-
Finnish
-
autosomaalisesti resessiivisesti periytyvät monirakkulaiset
-
autosomaalisesti resessiivisesti periytyvät monirakkulamunuaiset
-
autosomaalisesti resessiivisesti periytyvät polykystiset munuaiset
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infantiili munuaisten monirakkulatauti
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lapsuustyyppinen munuaisten monirakkulatauti
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morbus polycysticus renalis autosomaticus recessivus
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morbus polycysticus renalis infantilis
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Swedish
URI
http://www.yso.fi/onto/mesh/D017044
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