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complement component 4a deficiency
Human disease
C4A Deficiency
COMPLEMENT COMPONENT 4A DEFICIENCY
COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD
C4AD
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
29 November 2020
Disease Ontology ID
DOID:0060297
Complement 4 deficiency
0 references
genetic association
C4A
2 references
stated in
UniProt
UniProt protein ID
P0C0L4
retrieved
13 August 2019
stated in
Genetic analysis of C4 deficiency
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0060297
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0060297
http://identifiers.org/doid/DOID:0060297
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://www.orpha.net/ORDO/Orphanet_169147
0 references
Identifiers
MeSH descriptor ID
C565167
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0013721
Disease Ontology ID
DOID:0060297
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0060297
ICD-10-CM
D84.1
2 references
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060297
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0013721
Mondo ID
MONDO_0013721
0 references
OMIM ID
614380
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060297
614380
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0013721
Orphanet ID
169147
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0060297
UMLS CUI
C3280642
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0013721
C1852692
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0013721
UniProt disease ID
DI-01308
0 references
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(0 entries)
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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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