SHMARQL

nervous system heredodegenerative disease

<http://www.wikidata.org/entity/Q19001236>

human disease
rdfs:label
"nervous system heredodegenerative disease"@en
skos:altLabel
"Hereditary Neurodegenerative Disorder"@en
"Heredodegenerative Disorders, Nervous System"@en
"genetic neurodegenerative disease"@en
"hereditary neurodegenerative disease"@en
"inherited neurodegenerative disorder"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-23T23:33:42+00:00"^^xsd:dateTime
schema:version 2560156016
wikibase:identifiers 10
12
wikibase:sitelinks 0
wikibase:statements 113
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p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/D020271>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0024237>
p:direct-normalized/P672 <http://id.nlm.nih.gov/mesh/C10.574.500>
<http://id.nlm.nih.gov/mesh/C16.320.400>
p:direct-normalized/P8408 <http://kbpedia.org/kko/rc/NervousSystemHeredodegenerativeDisease>
wdt:P14914 "D183500"
wdt:P1550 "183500"
wdt:P1748 "C97073"
wdt:P1995 neurology
wdt:P2293 GARS1
GFAP
AR
VLDLR
FXN
PLP1
DAB1
ATN1
AARS1
KIF1A
SLC31A1
DARS1
EEF2
EIF2B1
FTH1
ASPA
FTL
GM2A
GRM1
HEXA
IGHMBP2
ITPR1
LETM1
MAL
ATXN3
MTTP
NAIP
PEX1
PEX6
PEX12
EXOSC9
ALDH18A1
Sodium–hydrogen antiporter 1
SMN2
VRK1
RNASET2
EIF2B3
EIF2B2
ZNHIT3
PEX16
ITM2B
TECPR2
ATG7
MTHFS
ERLIN1
KIF1C
AFG3L2
POLR3A
TREX1
EXOSC8
RPIA
SETX
SPART
ARL6IP1
RPGRIP1L
SLC44A1
DSTYK
ASCC1
EXOSC3
MECR
UBAP1
SPG21
TDP2
TMEM106B
GDAP2
POLR3B
VPS11
TWNK
GJC2
AARS2
ALS2
SLC5A7
VWA1
TMEM237
CSPP1
PANK2
COASY
RNASEH2C
GPT2
SELENOI
CEP41
NIPA1
CPT1C
LSM11
SAMD9L
HEPACAM
TMEM240
SLC35B2
CHCHD10
CCDC88C
ND2
CSF1R
ATP6
WARS1
wdt:P279 neurodegeneration
genetic nervous system disorder
wdt:P2892 "C0751870"
"C3273225"
"C5680568"
wdt:P31 type of disease
wdt:P486 "D020271"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0024237"
wdt:P672 "C10.574.500"
"C16.320.400"
wdt:P8408 "NervousSystemHeredodegenerativeDisease"
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data from SPARQL profile: Wikidata