(Q30899323)

English

CAKUT

urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux

Congenital anomalies of kidney and urinary tract
Renal or urinary tract malformation
Congenital anomalies of the kidney and urinary tract

In more languages

edit

Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

urinary system disease

1 reference

30 November 2020

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

genes associated with CAKUT

0 references

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0080205

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0080205

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

Identifiers

MeSH descriptor ID

C566906

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

1 reference

30 November 2020

0 references

1 reference

28 August 2019

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0019719

Sitelinks

Wikipedia(1 entry)

itwiki CAKUT

(Q30899323)

CAKUT

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)