(Q7080278)

English

Oguchi disease-1

human disease

CSNBO1
congenital stationary night blindness Oguchi type 1
Night Blindness, Congenital Stationary, Oguchi Type 1
Oguchi Disease type 1
OGUCHI DISEASE 1

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congenital stationary night blindness

1 reference

30 November 2020

1 reference

15 May 2019

autosomal recessive disease

1 reference

30 November 2020

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Mizuo–Nakamura phenomenon

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2 references

13 August 2019

A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese

on focus list of Wikimedia project

WikiProject Medicine

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exact match

http://purl.obolibrary.org/obo/DOID_0110712

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0110712

2 references

10 July 2020

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

http://www.orpha.net/ORDO/Orphanet_75382

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Identifiers

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1 reference

30 November 2020

1 reference

28 October 2013

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1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

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1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

6 August 2018

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mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

6 August 2018

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Sitelinks

Wikipedia(6 entries)

dewiki Oguchi-Syndrom
enwiki Oguchi disease
eswiki Enfermedad de Oguchi
plwiki Choroba Oguchiego
ruwiki Болезнь Огучи
ttwiki Тумыштагы стационар төнге сукырлык

(Q7080278)

Oguchi disease-1

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Identifiers

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Wikipedia(6 entries)

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