cerebellar ataxia

cerebellar disease characterized by ataxia originating in the cerebellum.
rdfs:label
"cerebellar ataxia"@en
skos:altLabel
"Ataxia, Cerebellar"@en
"Ataxias, Cerebellar"@en
"Cerebellar Ataxias"@en
"Cerebellar Dysmetria"@en
"Cerebellar Dysmetrias"@en
"ataxia"@en
"ataxia syndrome"@en
"rare ataxia"@en
"spinocerebellar ataxia"@en
schema:description
"cerebellar disease characterized by ataxia originating in the cerebellum."@en
schema:dateModified "2026-10-23T23:19:15+00:00"^^xsd:dateTime
schema:version 2560152443
wikibase:identifiers 31
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p:direct-normalized/P227 <https://d-nb.info/gnd/4338103-0>
p:direct-normalized/P244 <http://id.loc.gov/authorities/names/sh92003930>
p:direct-normalized/P2581 <http://babelnet.org/rdf/s02812028n>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D002524>
p:direct-normalized/P508 <http://purl.org/bncf/tid/79799>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0000437>
p:direct-normalized/P6366 <https://makg.org/entity/2780148635>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.228.140.252.190>
<http://id.nlm.nih.gov/mesh/C10.597.350.090.500>
<http://id.nlm.nih.gov/mesh/C23.888.592.350.090.200>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0050753>
wdt:P10283 "C2780148635"
wdt:P12385 "ataxia-cerebellosa"
wdt:P1296 "0161327"
wdt:P13204 "amufcqjx"
wdt:P1368 "000337108"
wdt:P1417 "science/cerebellar-ataxia"
wdt:P14914 "D102002"
wdt:P1550 "102002"
wdt:P1692 "334.3"
wdt:P1995 neurology
wdt:P227 "4338103-0"
wdt:P2293 FMR1
VLDLR
ATXN1
FXN
DNMT1
DAB1
ATN1
ATP1A3
CA8
EEF2
FGF14
TPP1
GJB1
GRID2
GRM1
ITPR1
KCNC3
KCND3
ATXN3
MTTP
NPTX1
PDYN
PEX6
PEX10
POU4F1
PPP2R2B
ATXN2
Sodium–hydrogen antiporter 1
SPTBN2
ELOVL4
TBCE
CACNA1G
CTDP1
PUM1
RUBCN
KIAA0586
STUB1
PITRM1
ATG7
AFG3L2
PNKP
SETX
PMPCA
CAMTA1
RPGRIP1L
PLEKHG4
TMEM216
TMEM138
TDP2
WWOX
ATP8A2
AHI1
GDAP2
MKS1
THG1L
ANO10
TWNK
SNX14
SCYL1
CC2D2A
SIL1
TMEM237
COA7
TMEM231
CSPP1
CEP290
PNPT1
CEP41
BEAN1
RNF168
SAMD9L
RNU12
TMEM240
TUBB2B
CCDC88C
wdt:P244 "sh92003930"
wdt:P2581 "02812028n"
wdt:P279 hereditary ataxia
cerebellar disease
wdt:P2888 <http://identifiers.org/doid/DOID:0050753>
<http://purl.obolibrary.org/obo/DOID_0050753>
<http://purl.obolibrary.org/obo/HP_0001251>
<http://www.orpha.net/ORDO/Orphanet_102002>
wdt:P2892 "C0007758"
"C5681771"
wdt:P31 type of disease
wdt:P373 "Cerebellar ataxia"
wdt:P3827 "cerebellar-ataxia"
wdt:P3841 "HP:0001251"
wdt:P4233 "cerebellar-ataxia"
wdt:P4317 "12060"
wdt:P486 "D002524"
wdt:P493 "334.3"
wdt:P494 "G11.1"
"G11.3"
wdt:P5008 WikiProject Medicine
wdt:P508 "79799"
wdt:P5270 "MONDO_0000437"
wdt:P557 "2218"
wdt:P604 "001397"
wdt:P6366 "2780148635"
wdt:P646 "/m/02vkcrn"
wdt:P667 "N99"
wdt:P672 "C10.228.140.252.190"
"C10.597.350.090.500"
"C23.888.592.350.090.200"
wdt:P699 "DOID:0050753"
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