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English
complement 3 deficiency
human disease
complement component 3 deficiency
C3 deficiency
C3D
C3 Deficiency, Autosomal Recessive
COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D
COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE
In more languages
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Statements
instance of
rare disease
0 references
class of disease
0 references
subclass of
complement deficiency
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:8354
immunodeficiency due to a complement cascade component deficiency
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013417
genetic association
C3
3 references
stated in
UniProt
UniProt protein ID
P01024
retrieved
13 August 2019
stated in
Molecular basis of polymorphisms of human complement component C3.
stated in
Open Targets Platform
retrieved
24 August 2023
reference URL
https://platform.opentargets.org/evidence/ENSG00000125730/MONDO_0013417
based on heuristic
inferred from an Open Targets association score over 0.7
on focus list of Wikimedia project
WikiProject Medicine
0 references
NCI Thesaurus ID
C9468
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:8354
exact match
http://purl.obolibrary.org/obo/DOID_8354
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:8354
http://identifiers.org/doid/DOID:8354
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://www.orpha.net/ORDO/Orphanet_280133
0 references
Identifiers
MeSH descriptor ID
C565169
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013417
Disease Ontology ID
DOID:8354
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:8354
DiseasesDB
1869
1 reference
imported from Wikimedia project
English Wikipedia
ICD-10-CM
D84.1
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013417
ICD-11 (foundation)
706642911
0 references
Microsoft Academic ID
2780360899
0 references
Mondo ID
MONDO_0013417
0 references
OMIM ID
613779
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:8354
Orphanet ID
280133
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:8354
UMLS CUI
C3151071
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0013417
C1332655
1 reference
stated in
Disease Ontology
retrieved
15 May 2019
Disease Ontology ID
DOID:8354
UniProt disease ID
DI-01307
0 references
Sitelinks
Wikipedia
(1 entry)
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enwiki
Complement 3 deficiency
Wikibooks
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Wikinews
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Wikisource
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Wikiversity
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Wikivoyage
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Wiktionary
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Multilingual sites
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