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(Q21082498)
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spastic ataxia
Human disease
SPAX
In more languages
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No label defined
No description defined
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Statements
instance of
class of disease
0 references
subclass of
hereditary ataxia
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0050952
health specialty
neurology
0 references
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0050952
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0050952
http://identifiers.org/doid/DOID:0050952
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://purl.obolibrary.org/obo/HP_0002497
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002497
http://www.orpha.net/ORDO/Orphanet_316226
0 references
Identifiers
MeSH descriptor ID
C564815
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0017845
C564815
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002497
KEGG ID
H01351
0 references
Disease Ontology ID
DOID:0050952
1 reference
stated in
Disease Ontology
retrieved
29 November 2020
Disease Ontology ID
DOID:0050952
Human Phenotype Ontology ID
HP:0002497
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002497
ICD-10 ID
G11.4
0 references
ICD-10-CM
G11.4
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0017845
Medical Dictionary for Regulatory Activities ID
10019903
1 reference
reference URL
https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx
based on heuristic
inferred by common ICD-10 mappings on Wikidata and on source
Mondo ID
MONDO_0017845
0 references
Orphanet ID
316226
0 references
316226
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0017845
UMLS CUI
C1849156
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
7 August 2018
Mondo ID
MONDO_0017845
C1849156
1 reference
stated in
Human Phenotype Ontology release 2018-03-08
retrieved
8 October 2018
Human Phenotype Ontology ID
HP:0002497
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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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