amyotrophic lateral sclerosis

rare neurodegenerative disease with amyotrophy and progressive paralysis

Wikidata entity: Q206901

Wikimedia Commons category is Amyotrophic lateral sclerosis

P689 afflicts ... Q1133903 (motor neuron) motor neuron
P373 Commons category String Amyotrophic lateral sclerosis ???
P2176 drug or therapy used for treatment ... Q335099 (edaravone) edaravone
P2176 drug or therapy used for treatment ... Q415744 (riluzole) riluzole
P2888 exact match Url None ???
P2888 exact match Url None ???
P2888 exact match Url None ???
P2888 exact match Url None ???
P1325 external data available at URL Url None ???
P2293 genetic association ... Q3944470 (ANXA3) ANXA3
P2293 genetic association ... Q14881694 (TBXAS1) TBXAS1
P2293 genetic association ... Q14882120 (ANG) ANG
P2293 genetic association ... Q14901671 (SELL) SELL
P2293 genetic association ... Q14905312 (MASP1) MASP1
P2293 genetic association ... Q14905515 (ATXN1) ATXN1
P2293 genetic association ... Q14908148 (EPB41) EPB41
P2293 genetic association ... Q15324395 (TRPM8) TRPM8
P2293 genetic association ... Q15328137 (SOD1) SOD1
P2293 genetic association ... Q17826316 (ANK3) ANK3
P2293 genetic association ... Q17833354 (ATP2B2) ATP2B2
P2293 genetic association ... Q17911616 (CTNND2) CTNND2
P2293 genetic association ... Q17912302 (DACH1) DACH1
P2293 genetic association ... Q17914420 (DPP6) DPP6
P2293 genetic association ... Q17917202 (ERBB4) ERBB4
P2293 genetic association ... Q18024775 (FUS) FUS
P2293 genetic association ... Q18027069 (HNRNPA1) HNRNPA1
P2293 genetic association ... Q18027222 (HOXD10) HOXD10
P2293 genetic association ... Q18027662 (IFRD1) IFRD1
P2293 genetic association ... Q18028022 (ITGA9) ITGA9
P2293 genetic association ... Q18028076 (ITPR2) ITPR2
P2293 genetic association ... Q18028441 (LAMA2) LAMA2
P2293 genetic association ... Q18028444 (LAMA3) LAMA3
P2293 genetic association ... Q18028510 (LDHC) LDHC
P2293 genetic association ... Q18030033 (NEK1) NEK1
P2293 genetic association ... Q18030071 (NFATC2) NFATC2
P2293 genetic association ... Q18030180 (CNOT2) CNOT2
P2293 genetic association ... Q18030391 (PCSK5) PCSK5
P2293 genetic association ... Q18030423 (PDGFRL) PDGFRL
P2293 genetic association ... Q18030490 (PFN1) PFN1
P2293 genetic association ... Q18030942 (PTPRF) PTPRF
P2293 genetic association ... Q18031501 (ST3GAL3) ST3GAL3
P2293 genetic association ... Q18031952 (TFAP2A) TFAP2A
P2293 genetic association ... Q18032223 (TUBA4A) TUBA4A
P2293 genetic association ... Q18032318 (VCP) VCP
P2293 genetic association ... Q18033146 (SLC25A12) SLC25A12
P2293 genetic association ... Q18033452 (INPP4B) INPP4B
P2293 genetic association ... Q18033497 (SQSTM1) SQSTM1
P2293 genetic association ... Q18033893 (ARHGEF2) ARHGEF2
P2293 genetic association ... Q18033922 (VAPB) VAPB
P2293 genetic association ... Q18034007 (B4GALT6) B4GALT6
P2293 genetic association ... Q18034037 (NRXN3) NRXN3
P2293 genetic association ... Q18034442 (ABCG1) ABCG1
P2293 genetic association ... Q18034504 (RGS6) RGS6
P2293 genetic association ... Q18034654 (KIAA0513) KIAA0513
P2293 genetic association ... Q18034860 (FIG4) FIG4
P2293 genetic association ... Q18034867 (RBM19) RBM19
P2293 genetic association ... Q18035056 (OPTN) OPTN
P2293 genetic association ... Q18035155 (KCNMB2) KCNMB2
P2293 genetic association ... Q18035471 (PROCR) PROCR
P2293 genetic association ... Q18035486 (OLFM4) OLFM4
P2293 genetic association ... Q18035901 (TSPAN9) TSPAN9
P2293 genetic association ... Q18036502 (MRAS) MRAS
P2293 genetic association ... Q18036594 (KIFAP3) KIFAP3
P2293 genetic association ... Q18036664 (UNC13A) UNC13A
P2293 genetic association ... Q18036734 (NFASC) NFASC
P2293 genetic association ... Q18037094 (NEDD4L) NEDD4L
P2293 genetic association ... Q18037179 (TARDBP) TARDBP
P2293 genetic association ... Q18037219 (ZFYVE26) ZFYVE26
P2293 genetic association ... Q18037847 (CHMP2B) CHMP2B
P2293 genetic association ... Q18039744 (UBQLN2) UBQLN2
P2293 genetic association ... Q18042006 (ZFP64) ZFP64
P2293 genetic association ... Q18042565 (ANKS1B) ANKS1B
P2293 genetic association ... Q18045667 (SUSD1) SUSD1
P2293 genetic association ... Q18047241 (CALN1) CALN1
P2293 genetic association ... Q18047482 (LRRC8C) LRRC8C
P2293 genetic association ... Q18047674 (NT5C1A) NT5C1A
P2293 genetic association ... Q18048815 (ABCC12) ABCC12
P2293 genetic association ... Q18049070 (TMEM132B) TMEM132B
P2293 genetic association ... Q18049268 (ARAP2) ARAP2
P2293 genetic association ... Q18050033 (CPNE4) CPNE4
P2293 genetic association ... Q18050827 (CHODL) CHODL
P2293 genetic association ... Q18050946 (MACROD2) MACROD2
P2293 genetic association ... Q18051591 (ANKRD29) ANKRD29
P2293 genetic association ... Q18052184 (CNTN4) CNTN4
P2293 genetic association ... Q18052989 (SYNPO2) SYNPO2
P2293 genetic association ... Q18053214 (SLC39A11) SLC39A11
P1995 health specialty ... Q83042 (neurology) neurology
P1692 ICD-9-CM String 335.20 ???
P667 ICPC 2 ID String N99 ???
P31 instance of ... Q929833 (rare disease) rare disease
P31 instance of ... Q42303753 (designated intractable/rare disease) designated intractable/rare disease
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q112965645 (symptom or sign) symptom or sign
P923 medical examination ... Q108525727 (Awaji Criteria) Awaji Criteria
P138 named after ... Q20710 (Jean-Martin Charcot) Jean-Martin Charcot
P138 named after ... Q357444 (Lou Gehrig) Lou Gehrig
P1748 NCI Thesaurus ID String C34373 ???
P1449 nickname Monolingualtext Lou Gehrig's disease ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P443 pronunciation audio CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/LL-Q33810%20%28ori%29-Psubhashish-%E0%AC%86%E0%AC%AE%E0%AC%BE%E0%AD%9F%E0%AD%8B%E0%AC%9F%E0%AD%8D%E0%AC%B0%E0%AD%8B%E0%AC%AB%E0%AC%BF%E0%AC%95%E0%AD%8D%20%E0%AC%B2%E0%AC%BE%E0%AC%9F%E0%AD%87%E0%AC%B0%E0%AC%BE%E0%AC%B2%20%E0%AC%B8%E0%AD%8D%E0%AC%95%E0%AD%8D%E0%AC%B2%E0%AD%87%E0%AC%B0%E0%AD%8B%E0%AC%B8%E0%AC%BF%E0%AC%B8%E0%AD%8D.wav ???
P1813 short name Monolingualtext ALS ???
P1813 short name Monolingualtext ELA ???
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q1225194 (monogenic disease) monogenic disease
P279 subclass of ... Q1755122 (neurodegeneration) neurodegeneration
P279 subclass of ... Q3221083 (motor neuron disease) motor neuron disease
P279 subclass of ... Q54920211 (TDP-43 Proteinopathies) TDP-43 Proteinopathies
P1424 topic has template ... Q20353203 (Template:Amyotrophic lateral sclerosis) Template:Amyotrophic lateral sclerosis
P910 topic's main category ... Q27811465 (Category:Amyotrophic lateral sclerosis) Category:Amyotrophic lateral sclerosis
External Ids
P8785AniDB tag ID847
P268Bibliothèque nationale de France ID12110754p
P508BNCF Thesaurus ID36605
P699Disease Ontology IDDOID:332
P557DiseasesDB29148
P673eMedicine ID1170097
P673eMedicine ID791154
P673eMedicine ID306543
P646Freebase ID/m/017s1k
P4317GARD rare disease ID5786
P668GeneReviews IDNBK1450
P7464Genetics Home Reference Conditions IDamyotrophic-lateral-sclerosis
P12385Gran Enciclopèdia Catalana IDesclerosi-lateral
P1296Gran Enciclopèdia Catalana ID (former scheme)0180358
P2924Great Russian Encyclopedia Online ID (old version)4424982
P3841Human Phenotype Ontology IDHP:0007354
P4229ICD-10-CMG12.2
P4229ICD-10-CMG12.21
P7807ICD-11 ID (Foundation)1982355687
P7329ICD-11 ID (MMS)8B60.0
P493ICD-9 ID335.20
P2074internetmedicin.se ID1054
P3827JSTOR topic ID (archived)amyotrophic-lateral-sclerosis
P8408KBpedia IDAmyotrophicLateralSclerosis
P665KEGG IDH00058
P6621Le Figaro tag IDmaladie-de-Charcot
P244Library of Congress authority IDsh85004728
P604MedlinePlus ID000688
P604MedlinePlus ID000688
P486MeSH descriptor IDD000690
P672MeSH tree codeC10.228.854.139
P672MeSH tree codeC10.574.562.250
P672MeSH tree codeC10.574.950.050
P672MeSH tree codeC10.668.467.250
P672MeSH tree codeC18.452.845.800.050
P5270Mondo IDMONDO_0004976
P8189National Library of Israel J9U ID987007294733105171
P1368National Library of Latvia ID000125199
P349NDL Authority ID01127913
P691NL CR AUT IDph397748
P492OMIM ID105400
P492OMIM ID105400
P10283OpenAlex IDC2778466831
P10283OpenAlex IDC2780596555
P1550Orphanet ID803
P1461Patientplus IDMotor-Neurone-Disease-(MND)
P4233PatientsLikeMe condition IDals
P3417Quora topic IDAmyotrophic-Lateral-Sclerosis-ALS
P5082Store medisinske leksikon IDALS_-_amyotrofisk_lateral_sklerose
P3984subredditALS
P4527UK Parliament thesaurus ID288352
P2892UMLS CUIC0002736
P2892UMLS CUIC0393554
P11430UniProt disease IDDI-00107
P12800Vikidia article IDfr:Maladie_de_Charcot
P12086WikiKids IDAmyotrofe_laterale_sclerose
P11143WikiProjectMed IDAmyotrophic lateral sclerosis
P11143WikiProjectMed IDMotor neuron disease
P3471WikiSkripta article ID31784
P13591Yale LUX IDconcept/4387b84a-327a-4da4-95bd-21f8333c5d08
P2347YSO ID8108

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