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spinocerebellar ataxia type 10
Human disease
SCA10
Spinocerebellar Ataxia type 10
SPINOCEREBELLAR ATAXIA 10
SPINOCEREBELLAR ATAXIA 10; SCA10
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No label defined
No description defined
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Statements
instance of
developmental defect during embryogenesis
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
28 July 2018
Mondo ID
MONDO_0011330
rare disease
0 references
class of disease
0 references
subclass of
spinocerebellar ataxia
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0050960
autosomal dominant cerebellar ataxia type IV
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0011330
genetic association
ATXN10
2 references
stated in
UniProt
UniProt protein ID
Q9UBB4
retrieved
13 August 2019
stated in
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
on focus list of Wikimedia project
WikiProject Medicine
0 references
exact match
http://purl.obolibrary.org/obo/DOID_0050960
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0050960
http://identifiers.org/doid/DOID:0050960
1 reference
stated in
Identifiers.org
reference URL
https://registry.identifiers.org/registry/doid
http://www.orpha.net/ORDO/Orphanet_98761
0 references
Identifiers
MeSH descriptor ID
C566874
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0011330
Disease Ontology ID
DOID:0050960
1 reference
stated in
Disease Ontology
retrieved
30 November 2020
Disease Ontology ID
DOID:0050960
GARD rare disease ID
10474
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0050960
ICD-10-CM
G11.2
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0011330
Mondo ID
MONDO_0011330
0 references
OMIM ID
603516
1 reference
stated in
Disease Ontology
retrieved
28 August 2019
Disease Ontology ID
DOID:0050960
Orphanet ID
98761
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0011330
UMLS CUI
C1963674
mapping relation type
close match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0011330
UniProt disease ID
DI-01073
0 references
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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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