Movatterモバイル変換
[0]
ホーム
URL:
画像なし
夜間モード
Jump to content
Main menu
Main menu
move to sidebar
hide
Navigation
Main page
Community portal
Project chat
Create a new Item
Recent changes
Random Item
Query Service
Nearby
Help
Special pages
Lexicographical data
Create a new Lexeme
Recent changes
Random Lexeme
Search
Search
English
Appearance
Donate
Create account
Log in
Personal tools
Donate
Create account
Log in
Pages for logged out editors
learn more
Contributions
Talk
cone-rod dystrophy 12
(Q32146137)
Item
Discussion
English
Read
View history
Tools
Tools
move to sidebar
hide
Actions
Read
View history
General
What links here
Related changes
Permanent link
Page information
Concept URI
Cite this page
Get shortened URL
Download QR code
Print/export
Create a book
Download as PDF
Printable version
In other projects
Appearance
move to sidebar
hide
From Wikidata
cone-rod dystrophy that has material basis in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15
CORD12
Cone-Rod Dystrophy type 12
CONE-ROD DYSTROPHY 12
CONE-ROD DYSTROPHY 12; CORD12
edit
Language
Label
Description
Also known as
default for all languages
No label defined
–
English
cone-rod dystrophy 12
cone-rod dystrophy that has material basis in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15
CORD12
Cone-Rod Dystrophy type 12
CONE-ROD DYSTROPHY 12
CONE-ROD DYSTROPHY 12; CORD12
Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
cone-rod dystrophy
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111019
genetic association
PROM1
2 references
stated in
UniProt
UniProt protein ID
O43490
retrieved
13 August 2019
stated in
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0111019
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111019
http://identifiers.org/doid/DOID:0111019
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
Identifiers
MeSH descriptor ID
C567206
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012983
Disease Ontology ID
DOID:0111019
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0111019
Mondo ID
MONDO_0012983
0 references
OMIM ID
612657
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0111019
UMLS CUI
C2675210
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0012983
UniProt disease ID
DI-00326
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
Retrieved from "
https://www.wikidata.org/w/index.php?title=Q32146137&oldid=2087298568
"
Search
Search
cone-rod dystrophy 12
(Q32146137)
Add topic
[8]
ページ先頭
©2009-2025
Movatter.jp