(Q32143660)

English

Usher syndrome type 2D

human disease

USH2D
Usher syndrome type IID
USHER SYNDROME, TYPE IID
USHER SYNDROME, TYPE IID; USH2D

In more languages

Statements

0 references

class of disease

0 references

Usher syndrome type 2

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

4 references

UniProt protein ID

13 August 2019

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

9 December 2020

https://search.clinicalgenome.org/kb/gene-validity/8151

25 January 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGCIEX:assertion_8151

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0110840

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0110840

2 references

Disease Ontology

10 July 2020

Disease Ontology ID

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_231178

0 references

http://www.orpha.net/ORDO/Orphanet_886

0 references

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

2 references

Disease Ontology

28 August 2019

Disease Ontology ID

Monarch Disease Ontology release 2018-06-29

6 August 2018

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(0 entries)

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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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