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(Q55223313)
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English
arthrogryposis
persistent flexure or contracture of a joint
Congenital Multiple Arthrogryposis
Congenital Multiple Arthrogryposes
Arthrogryposes, Congenital Multiple
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Statements
instance of
clinical sign
0 references
class of disease
0 references
subclass of
joint disorder
0 references
congenital contractures
0 references
health specialty
rheumatology
0 references
NCI Thesaurus ID
C84572
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0008779
exact match
http://purl.obolibrary.org/obo/HP_0002804
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002804
Identifiers
MeSH descriptor ID
D001176
mapping relation type
exact match
subject named as
Arthrogryposis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0008779
MeSH tree code
C05.550.150
0 references
C05.651.102
0 references
C05.660.077
0 references
C16.131.621.077
0 references
Experimental Factor Ontology ID
0003857
1 reference
based on heuristic
inferred by common MONDO mappings on source and on Wikidata
Human Phenotype Ontology ID
HP:0002804
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002804
ICD-11 (foundation)
1692487835
0 references
ICD-11 ID (MMS)
LD26.4
subject named as
Arthrogryposis syndromes
0 references
Mondo ID
MONDO_0008779
0 references
Orphanet ID
109007
0 references
UMLS CUI
C0003886
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
6 August 2018
Mondo ID
MONDO_0008779
C0003886
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002804
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