(Q24284111)

rare genetic renal disease

28 July 2018

0 references

0 references

1 reference

30 November 2020

1 reference

non-syndromic renal or urinary tract malformation

28 July 2018

Mondo ID

MONDO_0019637

1 reference

rare genetic developmental defect during embryogenesis

28 July 2018

Mondo ID

MONDO_0019637

1 reference

on focus list of Wikimedia project

28 July 2018

0 references

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0080204

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0080204

1 reference

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

Identifiers.org

reference URL

http://purl.obolibrary.org/obo/HP_0000089

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

http://www.orpha.net/ORDO/Orphanet_93101

HP:0000089

0 references

Identifiers

PatientsLikeMe condition ID

0 references

0 references

1 reference

30 November 2020

HP:0000089

2 references

Human Phenotype Ontology release 2018-03-08

28 July 2018

8 October 2018

0 references

1 reference

28 July 2018

1 reference

28 July 2018

1 reference

Medical Dictionary for Regulatory Activities ID

28 July 2018

0 references

MF54.2

Small kidney

0 references

10049102

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

0 references

1 reference

28 August 2019

mapping relation type

close match

1 reference

28 July 2018

mapping relation type

close match

1 reference

Human Phenotype Ontology release 2018-03-08

28 July 2018

1 reference

8 October 2018