(Q55345685)

English

autosomal dominant neovascular inflammatory vitreoretinopathy

human disease

VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI
Vitreoretinopathy, Neovascular Inflammatory, Autosomal Dominant
VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY
VRNI
Proliferative Vitreoretinopathy
ADNIV

In more languages

default values for all languages

No label defined

No description defined

edit

Statements

0 references

0 references

vitreoretinal degeneration

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration

ICD-9-CM

362.29

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

http://www.orpha.net/ORDO/Orphanet_329211

0 references

Identifiers

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

(Q55345685)

autosomal dominant neovascular inflammatory vitreoretinopathy

Statements

Identifiers

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)