(Q5811451)

(Redirected from Q18557956)

English

fundus dystrophy

human disease

Retinal Dystrophy
fundus dystrophies
retinal dystrophies

In more languages

Statements

class of disease

0 references

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

retinal degeneration

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

genetic vitreous-retinal disease

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

health specialty

0 references

genetic association

1 reference

27 December 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_d8c69db5-8d29-40af-85f0-59471ce0c62c-2021-06-03T170000.000Z

1 reference

7 March 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_5399fd62-ca69-4665-b3ba-c15ceefbf6d9-2021-09-03T164559.434Z

1 reference

18 April 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_ece57d88-4307-420a-aedb-4b5900248ea1-2021-10-07T160000.000Z

1 reference

1 November 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_375ffa04-a8d9-427e-8948-f913bc8ff68d-2021-10-26T142732.609Z

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000165588/Orphanet_71862

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

362.75

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

362.72

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

NCI Thesaurus ID

C35625

mapping relation type

2 references

Disease Ontology

11 July 2018

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

28 July 2018

C35625

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

http://purl.obolibrary.org/obo/DOID_8501

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:8501

1 reference

Identifiers.org

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

http://purl.obolibrary.org/obo/HP_0000556

1 reference

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

http://www.orpha.net/ORDO/Orphanet_71862

0 references

Identifiers

MeSH descriptor ID

mapping relation type

subject named as

Retinal Dystrophies

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

C11.768.585.658

0 references

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

1 reference

imported from Wikimedia project

Spanish Wikipedia

Human Phenotype Ontology ID

2 references

Monarch Disease Ontology release 2018-06-29

28 July 2018

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

2 references

Disease Ontology

15 May 2019

Disease Ontology ID

Human Phenotype Ontology release 2018-03-08

8 October 2018

Human Phenotype Ontology ID

Sitelinks

Wikipedia(2 entries)

dewiki Netzhautdystrophie
eswiki Distrofias de la retina

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)

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