Polycystic Kidney, Autosomal Recessive [polycystické ledviny autozomálně recesivní]
- Terms
-
autozomálně recesivní polycystická choroba ledvin
autozomálně recesivní polycystické ledviny
infantilní polycystická choroba ledvin, typ 1
infantilní polycystické ledviny, typ 1
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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
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.
- DUI
- D017044 MeSH Browser
- CUI
- M0025899
- Previous indexing
- Kidney, Polycystic (1966-1991)
- History note
- 1992
- Public note
- 1992; see KIDNEY, POLYCYCSTIC, AUTOSOMAL RECESSIVE 1992-2000
Allowable subheadings
- BL
- blood 1
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 1
- CO
- complications 4
- DI
- diagnosis 16
- DG
- diagnostic imaging 2
- DH
- diet therapy
- DT
- drug therapy 2
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 3
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 10
- HI
- history
- IM
- immunology
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality 1
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology 4
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 8
- UR
- urine
- VE
- veterinary
- VI
- virology
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