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Cakut MeSH Supplementary Concept Data 2022


MeSH Supplementary
Cakut
Unique ID
C566906
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566906
Entry Term(s)
Congenital Anomalies Of Kidney And Urinary Tract
Registry Number
0
Heading Mapped to
*Urogenital Abnormalities
*Vesico-Ureteral Reflux
Frequency
109
Note
A range of renal and urinary tract malformations that vary from complete renal agenesis , to renal hypodysplasia, MULTICYSTIC DYSPLASTIC KIDNEY, duplex renal collecting system, ureteropelvic junction obstruction (UPJO), megaureter, posterior urethral valves (PUV), and vesicoureteral reflux (VUR). Up to 10% of cases are familial (autosomal dominant), although these are frequently asymptomatic or less severe; thus, PENETRANCE is incomplete. CAKUT occurs in 1 in 500 live births, and is lethal 1 in 2,000 births, it can also occur with other congenital anomalies, such as papillorenal syndrome (OMIM: 120330). OMIM: 610805
Date of Entry
2012/11/05
Revision Date
2015/08/17
Cakut Preferred
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