Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q53661599)
Watch
English
exudative vitreoretinopathy 7
human disease
EVR7
EXUDATIVE VITREORETINOPATHY 7; EVR7
In more languages
default values for all languages
No label defined
No description defined
edit
Statements
instance of
class of disease
0 references
subclass of
exudative vitreoretinopathy
2 references
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0033123
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0080264
autosomal dominant disease
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0080264
genetic association
CTNNB1
2 references
stated in
UniProt
UniProt protein ID
P35222
retrieved
13 August 2019
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000168036/Orphanet_891
based on heuristic
inferred from an Open Targets association score over 0.7
TSPAN12
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000106025/Orphanet_891
based on heuristic
inferred from an Open Targets association score over 0.7
NDP
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000124479/Orphanet_891
based on heuristic
inferred from an Open Targets association score over 0.7
LRP5
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000162337/Orphanet_891
based on heuristic
inferred from an Open Targets association score over 0.7
FZD4
1 reference
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000174804/Orphanet_891
based on heuristic
inferred from an Open Targets association score over 0.7
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0080264
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0080264
http://www.orpha.net/ORDO/Orphanet_891
0 references
http://identifiers.org/doid/DOID:0080264
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
Disease Ontology ID
DOID:0080264
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0080264
Mondo ID
MONDO_0033123
0 references
OMIM ID
617572
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0080264
Orphanet ID
891
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0033123
UMLS CUI
C4539767
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0033123
UniProt disease ID
DI-05042
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
