(Q55788175)

English

fetal lower urinary tract obstruction

human disease

LUTO

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

class of disease

0 references

rare genetic renal disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

rare genetic developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

rare genetic urogenital disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

urogenital tract malformation

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

urinary tract obstruction

0 references

http://www.orpha.net/ORDO/Orphanet_435365

0 references

Identifiers

ICD-11 (foundation)

0 references

ICD-11 ID (MMS)

LB31.2

subject named as

Fetal lower urinary tract obstruction

0 references

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

Sitelinks

Wikipedia(0 entries)

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q55788175&oldid=2088056361"