Scléaróis chliathánach amatrófach (Q206901)

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Galar is cúis le bás néarón

• ALS
• galad Lou Gehrig
• galar néarón luadrach

Language	Label	Description	Also known as
Gaeilge	Scléaróis chliathánach amatrófach	Galar is cúis le bás néarón	ALS galad Lou Gehrig galar néarón luadrach
Béarla	amyotrophic lateral sclerosis	rare neurodegenerative disease with amyotrophy and progressive paralysis	ALS Lou Gehrig's disease motor neuron disease, bulbar Lou Gehrig disease Charcot disease Amyotrophic lateral sclerosis motor neurone disease

Statements

sampla de

designated intractable/rare disease ^Béarla

3 references

URL tagartha

http://www.mhlw.go.jp/english/wp/wp-hw10/dl/02e.pdf

dáta rochtana

6 Nollaig 2018

URL tagartha

http://www.nanbyou.or.jp/entry/52

dáta rochtana

6 Nollaig 2018

URL tagartha

https://ddrare.nibiohn.go.jp/

dáta rochtana

17 Bealtaine 2019

galar neamhchoitianta

0 references

galar (aicme)

0 references

symptom or sign ^Béarla

0 references

fo-aicme de

Galar néarón luadrach

3 references

ráite i

Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neurons. ^Béarla

ráite i

Measurement of spinal cord atrophy using phase sensitive inversion recovery (PSIR) imaging in motor neuron disease ^Béarla

ráite i

Disease Ontology ^Béarla

dáta rochtana

30 Samhain 2020

Disease Ontology ID ^Béarla

DOID:332

TDP-43 Proteinopathies ^Béarla

0 references

néaraimheathlúchán

1 reference

ráite i

Monarch Disease Ontology release 2018-06-29 ^Béarla

dáta rochtana

3 Iúil 2018

Mondo ID ^Béarla

MONDO_0004976

galar aonghineach

1 reference

ráite i

Disease Ontology ^Béarla

dáta rochtana

30 Samhain 2020

Disease Ontology ID ^Béarla

DOID:332

galar

0 references

íomhá

ALS Coronal.jpg
920 × 938; 102 KB

1 reference

iompórtáilte ó thionscadal Vicipéide

Russian Wikipedia ^Béarla

leasainm

Lou Gehrig's disease (Béarla)

1 reference

URL tagartha

https://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis

ainm gearr

ELA (Catalóinis)

0 references

ALS (Béarla)

0 references

gearrthóg fuaime

LL-Q33810 (ori)-Psubhashish-ଆମାୟୋଟ୍ରୋଫିକ୍ ଲାଟେରାଲ ସ୍କ୍ଲେରୋସିସ୍.wav
3.3 s; 307 KB

teanga an tsaothair nó an ainm

Oirísis

1 reference

URL tagartha

https://lingualibre.org/wiki/Q648173

ainmnithe in ómós

Lou Gehrig

0 references

Jean-Martin Charcot

0 references

buaileann sé/sí

motor neuron ^Béarla

0 references

speisialtacht sláinte

néareolaíocht

0 references

medical examination ^Béarla

Awaji Criteria ^Béarla

0 references

druga a úsáidtear mar chóir leighis

riluzole ^Béarla

2 references

ráite i

NDF-RT ^Béarla

NDF-RT ID ^Béarla

N0000148421

teanga an tsaothair nó an ainm

Béarla

dáta rochtana

13 Nollaig 2016

ráite i

Drug Indications Extracted from FAERS ^Béarla

dáta rochtana

2 Deireadh Fómhair 2018

edaravone ^Béarla

1 reference

ráite i

Drug Indications Extracted from FAERS ^Béarla

dáta rochtana

2 Deireadh Fómhair 2018

riluzole ^Béarla

am tosaigh

12 Nollaig 1995

approved by ^Béarla

Riarachán Bia is Drugaí

1 reference

ráite i

Inxight: Drugs Database ^Béarla

dáta rochtana

2 Samhain 2018

URL tagartha

https://drugs.ncats.io/drug/7LJ087RS6F

https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=10c8d5e6-cb9f-402d-ab8e-65c1aa049e89

edaravone ^Béarla

am tosaigh

14 Eanáir 2010

approved by ^Béarla

Riarachán Bia is Drugaí

1 reference

ráite i

Inxight: Drugs Database ^Béarla

dáta rochtana

2 Samhain 2018

URL tagartha

https://drugs.ncats.io/drug/S798V6YJRP

http://www.e-search.ne.jp/~jpr/PDF/MT18.PDF

genetic association ^Béarla

ITGA9

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3680

http://www.genome.gov/gwastudies/index.cfm?gene=ITGA9

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

CTNND2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=1501

http://www.genome.gov/gwastudies/index.cfm?gene=CTNND2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

TSPAN9

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=10867

http://www.genome.gov/gwastudies/index.cfm?gene=TSPAN9

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

TFAP2A

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=7020

http://www.genome.gov/gwastudies/index.cfm?gene=TFAP2A

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ATP2B2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=491

http://www.genome.gov/gwastudies/index.cfm?gene=ATP2B2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

EPB41

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=2035

http://www.genome.gov/gwastudies/index.cfm?gene=EPB41

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

LRRC8C

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=84230

http://www.genome.gov/gwastudies/index.cfm?gene=LRRC8C

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

NFASC

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=23114

http://www.genome.gov/gwastudies/index.cfm?gene=NFASC

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

SLC25A12

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=8604

http://www.genome.gov/gwastudies/index.cfm?gene=SLC25A12

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ERBB4

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=2066

http://www.genome.gov/gwastudies/index.cfm?gene=ERBB4

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

14 Márta 2020

TRPM8

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=79054

http://www.genome.gov/gwastudies/index.cfm?gene=TRPM8

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

KCNMB2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=10242

http://www.genome.gov/gwastudies/index.cfm?gene=KCNMB2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

MASP1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=5648

http://www.genome.gov/gwastudies/index.cfm?gene=MASP1

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ANXA3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=306

http://www.genome.gov/gwastudies/index.cfm?gene=ANXA3

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

SYNPO2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=171024

http://www.genome.gov/gwastudies/index.cfm?gene=SYNPO2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

INPP4B

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=8821

http://www.genome.gov/gwastudies/index.cfm?gene=INPP4B

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

LAMA2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3908

http://www.genome.gov/gwastudies/index.cfm?gene=LAMA2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

CALN1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=83698

http://www.genome.gov/gwastudies/index.cfm?gene=CALN1

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

TBXAS1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=6916

http://www.genome.gov/gwastudies/index.cfm?gene=TBXAS1

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

PDGFRL

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=5157

http://www.genome.gov/gwastudies/index.cfm?gene=PDGFRL

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ANK3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=288

http://www.genome.gov/gwastudies/index.cfm?gene=ANK3

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

LDHC

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3948

http://www.genome.gov/gwastudies/index.cfm?gene=LDHC

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

RBM19

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9904

http://www.genome.gov/gwastudies/index.cfm?gene=RBM19

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

TMEM132B

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=114795

http://www.genome.gov/gwastudies/index.cfm?gene=TMEM132B

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

OLFM4

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=10562

http://www.genome.gov/gwastudies/index.cfm?gene=OLFM4

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

DACH1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=1602

http://www.genome.gov/gwastudies/index.cfm?gene=DACH1

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ZFYVE26

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=23503

http://www.genome.gov/gwastudies/index.cfm?gene=ZFYVE26

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

RGS6

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9628

http://www.genome.gov/gwastudies/index.cfm?gene=RGS6

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ABCC12

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=94160

http://www.genome.gov/gwastudies/index.cfm?gene=ABCC12

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

NEDD4L

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=23327

http://www.genome.gov/gwastudies/index.cfm?gene=NEDD4L

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

MACROD2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=140733

http://www.genome.gov/gwastudies/index.cfm?gene=MACROD2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

PROCR

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=10544

http://www.genome.gov/gwastudies/index.cfm?gene=PROCR

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

NFATC2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=4773

http://www.genome.gov/gwastudies/index.cfm?gene=NFATC2

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

CHODL

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=140578

http://www.genome.gov/gwastudies/index.cfm?gene=CHODL

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

HOXD10

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3236

http://www.genome.gov/gwastudies/index.cfm?gene=HOXD10

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

MRAS

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=22808

http://www.genome.gov/gwastudies/index.cfm?gene=MRAS

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ABCG1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9619

http://www.genome.gov/gwastudies/index.cfm?gene=ABCG1

ráite i

Phenocarta ^Béarla

Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations ^Béarla

dáta rochtana

25 Bealtaine 2020

ANKRD29

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=147463

http://www.genome.gov/gwastudies/index.cfm?gene=ANKRD29

ráite i

Phenocarta ^Béarla

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

UNC13A

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=23025

http://www.genome.gov/gwastudies/index.cfm?gene=UNC13A

ráite i

Phenocarta ^Béarla

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

CPNE4

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=131034

http://www.genome.gov/gwastudies/index.cfm?gene=CPNE4

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

KIAA0513

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9764

http://www.genome.gov/gwastudies/index.cfm?gene=KIAA0513

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

LAMA3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3909

http://www.genome.gov/gwastudies/index.cfm?gene=LAMA3

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

ST3GAL3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=6487

http://www.genome.gov/gwastudies/index.cfm?gene=ST3GAL3

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

ARHGEF2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9181

http://www.genome.gov/gwastudies/index.cfm?gene=ARHGEF2

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

PTPRF

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=5792

http://www.genome.gov/gwastudies/index.cfm?gene=PTPRF

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

ARAP2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=116984

http://www.genome.gov/gwastudies/index.cfm?gene=ARAP2

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

IFRD1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3475

http://www.genome.gov/gwastudies/index.cfm?gene=IFRD1

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

PCSK5

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=5125

http://www.genome.gov/gwastudies/index.cfm?gene=PCSK5

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

CNOT2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=4848

http://www.genome.gov/gwastudies/index.cfm?gene=CNOT2

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

ANKS1B

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=56899

http://www.genome.gov/gwastudies/index.cfm?gene=ANKS1B

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

18 Feabhra 2020

NRXN3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9369

http://www.genome.gov/gwastudies/index.cfm?gene=NRXN3

ráite i

Phenocarta ^Béarla

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. ^Béarla

dáta rochtana

25 Bealtaine 2020

B4GALT6

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=9331

http://www.genome.gov/gwastudies/index.cfm?gene=B4GALT6

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

NT5C1A

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=84618

http://www.genome.gov/gwastudies/index.cfm?gene=NT5C1A

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

SLC39A11

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=201266

http://www.genome.gov/gwastudies/index.cfm?gene=SLC39A11

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

ATXN1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=6310

http://www.genome.gov/gwastudies/index.cfm?gene=ATXN1

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

CNTN4

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=152330

http://www.genome.gov/gwastudies/index.cfm?gene=CNTN4

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

KIFAP3

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=22920

http://www.genome.gov/gwastudies/index.cfm?gene=KIFAP3

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

SELL

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=6402

http://www.genome.gov/gwastudies/index.cfm?gene=SELL

ráite i

Phenocarta ^Béarla

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis ^Béarla

dáta rochtana

25 Bealtaine 2020

DPP6

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=1804

http://www.genome.gov/gwastudies/index.cfm?gene=DPP6

ráite i

Phenocarta ^Béarla

Screening for replication of genome-wide SNP associations in sporadic ALS ^Béarla

dáta rochtana

25 Bealtaine 2020

ITPR2

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=3709

http://www.genome.gov/gwastudies/index.cfm?gene=ITPR2

ráite i

Phenocarta ^Béarla

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study ^Béarla

dáta rochtana

25 Bealtaine 2020

ZFP64

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=55734

http://www.genome.gov/gwastudies/index.cfm?gene=ZFP64

ráite i

Phenocarta ^Béarla

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data ^Béarla

dáta rochtana

25 Bealtaine 2020

SUSD1

determination method ^Béarla

genome-wide association study ^Béarla

TAS ^Béarla

1 reference

URL tagartha

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_332&ncbiId=64420

http://www.genome.gov/gwastudies/index.cfm?gene=SUSD1

ráite i

Phenocarta ^Béarla

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data ^Béarla

dáta rochtana

25 Bealtaine 2020

NEK1

1 reference

DOI

10.1038/NG.3626

SQSTM1

1 reference

ráite i

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis ^Béarla

ANG

1 reference

ráite i

A novel candidate region for ALS on chromosome 14q11.2. ^Béarla

TARDBP

3 references

ráite i

Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations ^Béarla

ráite i

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis ^Béarla

ráite i

Open Targets Platform ^Béarla

dáta rochtana

24 Lúnasa 2023

URL tagartha

https://platform.opentargets.org/evidence/ENSG00000120948/MONDO_0004976

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

TUBA4A

1 reference

ráite i

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. ^Béarla

FIG4

2 references

ráite i

Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS. ^Béarla

ráite i

Open Targets Platform ^Béarla

dáta rochtana

24 Lúnasa 2023

URL tagartha

https://platform.opentargets.org/evidence/ENSG00000112367/MONDO_0004976

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

OPTN

2 references

ráite i

Mutations of optineurin in amyotrophic lateral sclerosis ^Béarla

ráite i

Open Targets Platform ^Béarla

dáta rochtana

24 Lúnasa 2023

URL tagartha

https://platform.opentargets.org/evidence/ENSG00000123240/MONDO_0004976

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

FUS

1 reference

ráite i

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis ^Béarla

SOD1

2 references

ráite i

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis ^Béarla

ráite i

Open Targets Platform ^Béarla

dáta rochtana

24 Lúnasa 2023

URL tagartha

https://platform.opentargets.org/evidence/ENSG00000142168/MONDO_0004976

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

VCP

2 references

ráite i

Exome sequencing reveals VCP mutations as a cause of familial ALS ^Béarla

ráite i

Open Targets Platform ^Béarla

dáta rochtana

24 Lúnasa 2023

URL tagartha

https://platform.opentargets.org/evidence/ENSG00000165280/MONDO_0004976

bunaithe ar chur chuige heorastúil

inferred from an Open Targets association score over 0.7 ^Béarla

HNRNPA1

1 reference

ráite i

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS ^Béarla

PFN1

1 reference

ráite i

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis ^Béarla

UBQLN2

1 reference

ráite i

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia ^Béarla

VAPB

1 reference

ráite i

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis ^Béarla

CHMP2B

1 reference

ráite i

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B) ^Béarla

external data available at URL ^Béarla

http://www.nanbyou.or.jp/entry/52

teanga an tsaothair nó an ainm

an tSeapáinis

1 reference

URL tagartha

https://ddrare.nibiohn.go.jp/

dáta rochtana

17 Bealtaine 2019

on focus list of Wikimedia project ^Béarla

WikiProject Medicine ^Béarla

0 references

ICD-9-CM ^Béarla

335.20

2 references

ráite i

Disease Ontology ^Béarla

dáta rochtana

15 Bealtaine 2019

Disease Ontology ID ^Béarla

DOID:332

ráite i

Monarch Disease Ontology release 2018-06-29 ^Béarla

dáta rochtana

3 Iúil 2018

Mondo ID ^Béarla

MONDO_0004976

ICPC 2 ID ^Béarla

N99

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid na Spáinnise

NCI Thesaurus ID ^Béarla

C34373

1 reference

ráite i

Disease Ontology ^Béarla

dáta rochtana

15 Bealtaine 2019

Disease Ontology ID ^Béarla

DOID:332

exact match ^Béarla

http://purl.obolibrary.org/obo/DOID_332

1 reference

ráite i

Disease Ontology ^Béarla

dáta rochtana

30 Samhain 2020

Disease Ontology ID ^Béarla

DOID:332

http://identifiers.org/doid/DOID:332

1 reference

ráite i

Identifiers.org ^Béarla

URL tagartha

https://registry.identifiers.org/registry/doid

http://purl.obolibrary.org/obo/HP_0007354

1 reference

ráite i

Human Phenotype Ontology release 2018-03-08 ^Béarla

dáta rochtana

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

HP:0007354

http://www.orpha.net/ORDO/Orphanet_803

0 references

catagóir Commons

Amyotrophic lateral sclerosis

0 references

príomhtheimpléad na topaice

Template:Amyotrophic lateral sclerosis ^Béarla

1 reference

inferred from ^Béarla

Template:Amyotrophic lateral sclerosis ^Béarla

príomhchatagóir na topaice

Category:Amyotrophic lateral sclerosis ^Béarla

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

Identifiers

Bibliothèque nationale de France ID ^Béarla

12110754p

0 references

National Library of Israel J9U ID ^Béarla

987007294733105171

1 reference

ráite i

Leabharlann Náisiúnta Iosrael

aitheantóir LoC

sh85004728

0 references

National Library of Latvia ID ^Béarla

000125199

0 references

NDL Authority ID ^Béarla

01127913

0 references

NL CR AUT ID ^Béarla

ph397748

luaite mar

amyotrofická laterální skleróza

0 references

MeSH descriptor ID ^Béarla

D000690

mapping relation type ^Béarla

exact match ^Béarla

luaite mar

Amyotrophic Lateral Sclerosis

1 reference

ráite i

Monarch Disease Ontology release 2018-06-29 ^Béarla

dáta rochtana

3 Iúil 2018

Mondo ID ^Béarla

MONDO_0004976

MeSH tree code ^Béarla

C10.228.854.139

0 references

C10.574.562.250

0 references

C10.574.950.050

0 references

C10.668.467.250

0 references

C18.452.845.800.050

0 references

ID MedlinePlus

000688

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

PatientsLikeMe condition ID ^Béarla

als

0 references

KEGG ID ^Béarla

H00058

0 references

AniDB tag ID ^Béarla

847

0 references

BBC Things ID ^Béarla

6c2f0633-2664-4233-ba56-5ce53cb764f9

1 reference

ráite i

BBC Things ^Béarla

BNCF Thesaurus ID ^Béarla

36605

1 reference

ráite i

National Central Library of Florence ^Béarla

Disease Ontology ID ^Béarla

DOID:332

1 reference

ráite i

Disease Ontology ^Béarla

dáta rochtana

30 Samhain 2020

Disease Ontology ID ^Béarla

DOID:332

DiseasesDB ^Béarla

29148

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

eMedicine ID ^Béarla

1170097

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

791154

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

306543

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

Freebase ID ^Béarla

/m/017s1k

1 reference

ráite i

Freebase Data Dumps ^Béarla

dáta foilsithe

28 Deireadh Fómhair 2013

French Vikidia ID ^Béarla

Maladie_de_Charcot

0 references

GARD rare disease ID ^Béarla

5786

0 references

Genetics Home Reference Conditions ID ^Béarla

amyotrophic-lateral-sclerosis

0 references

Gran Enciclopèdia Catalana ID ^Béarla

esclerosi-lateral

0 references

ID Gran Enciclopèdia Catalana

0180358

0 references

Great Russian Encyclopedia Online ID (old version) ^Béarla

4424982

luaite mar

АМИОТРОФИЧЕСКИЙ БОКОВОЙ СКЛЕРОЗ

0 references

1818344

reason for deprecated rank ^Béarla

atreorú

0 references

Human Phenotype Ontology ID ^Béarla

HP:0007354

1 reference

ráite i

Human Phenotype Ontology release 2018-03-08 ^Béarla

dáta rochtana

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

HP:0007354

ICD-10-CM ^Béarla

G12.21

2 references

ráite i

Disease Ontology ^Béarla

dáta rochtana

15 Bealtaine 2019

Disease Ontology ID ^Béarla

DOID:332

ráite i

Monarch Disease Ontology release 2018-06-29 ^Béarla

dáta rochtana

3 Iúil 2018

Mondo ID ^Béarla

MONDO_0004976

G12.2

1 reference

ráite i

Monarch Disease Ontology release 2018-06-29 ^Béarla

dáta rochtana

3 Iúil 2018

Mondo ID ^Béarla

MONDO_0004976

ICD-11 (foundation) ^Béarla

1982355687

0 references

ICD-11 ID (MMS) ^Béarla

8B60.0

luaite mar

Amyotrophic lateral sclerosis

0 references

ICD-9 ID ^Béarla

335.20

1 reference

iompórtáilte ó thionscadal Vicipéide

Russian Wikipedia ^Béarla

Wikimedia import URL ^Béarla

https://ru.wikipedia.org/?oldid=131108756

internetmedicin.se ID ^Béarla

1054

1 reference

iompórtáilte ó thionscadal Vicipéide

Swedish Wikipedia ^Béarla

JSTOR topic ID ^Béarla

amyotrophic-lateral-sclerosis

0 references

KBpedia ID ^Béarla

AmyotrophicLateralSclerosis

1 reference

ráite i

KBpedia

dáta rochtana

9 Iúil 2020

Le Figaro tag ID ^Béarla

maladie-de-Charcot

0 references

Mondo ID ^Béarla

MONDO_0004976

0 references

OMIM ID ^Béarla

105400

1 reference

iompórtáilte ó thionscadal Vicipéide

Vicipéid an Bhéarla

Wikimedia import URL ^Béarla

https://en.wikipedia.org/w/index.php?title=Amyotrophic_lateral_sclerosis&oldid=954719609

OpenAlex ID ^Béarla

C2778466831

1 reference

ráite i

OpenAlex ^Béarla

dáta rochtana

26 Eanáir 2022

URL tagartha

https://docs.openalex.org/download-snapshot/snapshot-data-format

C2780596555

1 reference

ráite i

OpenAlex ^Béarla

dáta rochtana

26 Eanáir 2022

URL tagartha

https://docs.openalex.org/download-snapshot/snapshot-data-format

Orphanet ID ^Béarla

803

1 reference

ráite i

Disease Ontology ^Béarla

dáta rochtana

15 Bealtaine 2019

Disease Ontology ID ^Béarla

DOID:332

Patientplus ID ^Béarla

Motor-Neurone-Disease-(MND)

1 reference

URL tagartha

http://www.patient.co.uk/patientplus/a.htm

ID na topaice ar Quora

Amyotrophic-Lateral-Sclerosis-ALS

0 references

Store medisinske leksikon ID ^Béarla

ALS_-_amyotrofisk_lateral_sklerose

0 references

subreddit ^Béarla

ALS

1 reference

URL tagartha

https://old.reddit.com/r/ALS/

teideal

ALS (Béarla)

dáta rochtana

28 Samhain 2021

UK Parliament thesaurus ID ^Béarla

288352

luaite mar

Motor neurone disease

0 references

UMLS CUI ^Béarla

C0002736

2 references

ráite i

Disease Ontology ^Béarla

dáta rochtana

15 Bealtaine 2019

Disease Ontology ID ^Béarla

DOID:332

ráite i

Human Phenotype Ontology release 2018-03-08 ^Béarla

dáta rochtana

8 Deireadh Fómhair 2018

Human Phenotype Ontology ID ^Béarla

HP:0007354

C0393554

1 reference

bunaithe ar chur chuige heorastúil

inferred by common MeSH mappings on source and on Wikidata ^Béarla

ráite i

UMLS 2023 ^Béarla

dáta rochtana

25 Bealtaine 2023

UniProt disease ID ^Béarla

DI-00107

0 references

WikiKids ID ^Béarla

Amyotrofe_laterale_sclerose

0 references

WikiProjectMed ID ^Béarla

Amyotrophic lateral sclerosis

0 references

WikiSkripta article ID ^Béarla

31784

0 references

YSO ID ^Béarla

8108

1 reference

ráite i

YSO-Wikidata mapping project ^Béarla

 

Sitelinks

Vicipéid(68 entries)

• afwiki Motorneuronsiekte
• arwiki تصلب جانبي ضموري
• astwiki Esclerosis llateral amiotrófica
• azbwiki آموتروفیک لیترال
• azwiki Yan amiotrofik skleroz
• bgwiki Амиотрофична латерална склероза
• bswiki ALS4
• cawiki Esclerosi lateral amiotròfica
• ckbwiki ئامیۆترۆفیک لاتێرال سکلێرۆزیس
• cswiki Amyotrofická laterální skleróza
• dawiki Amyotrofisk lateral sklerose
• dewiki Amyotrophe Lateralsklerose
• elwiki Αμυοτροφική πλευρική σκλήρυνση
• enwiki ALS
• eowiki Amiotrofa lateralsklerozo
• eswiki Esclerosis lateral amiotrófica
• etwiki Amüotroofne lateraalskleroos
• euwiki Alboko esklerosi amiotrofiko
• fawiki اسکلروز جانبی آمیوتروفیک
• fiwiki ALS-tauti
• frwiki Sclérose latérale amyotrophique
• gawiki Scléaróis chliathánach amatrófach
• glwiki Esclerose lateral amiotrófica
• hewiki טרשת אמיוטרופית צידית
• hiwiki पेशीशोषी पार्श्व काठिन्य (एमियोट्रॉफ़िक लैटरल स्कलिरॉसिस)
• hrwiki Amiotrofična lateralna skleroza
• huwiki Amiotrófiás laterálszklerózis
• hywiki Կողմնային ամիոտրոֆիկ սկլերոզ
• idwiki Sklerosis lateral amiotrofik
• iswiki Lou Gehrig-sjúkdómur
• itwiki Sclerosi laterale amiotrofica
• jawiki 筋萎縮性側索硬化症
• kawiki ამიოტროფული გვერდითი სკლეროზი
• kowiki 근위축성 측삭경화증
• lawiki Sclerosis lateralis amyotrophica
• lbwiki Amyotroph Lateral Skleros
• liwiki ALS
• lvwiki Amiotrofā laterālā skleroze
• mkwiki Амиотрофична латерална склероза
• mlwiki അമിട്രോഫിക് ലാറ്ററൽ സ്‌ക്ലീറോസിസ്
• mswiki Sklerosis lateral amiotrofik
• nlwiki Amyotrofe laterale sclerose
• nowiki Amyotrofisk lateralsklerose
• orwiki ଆମାୟୋଟ୍ରୋଫିକ୍ ଲାଟେରାଲ ସ୍କ୍ଲେରୋସିସ୍
• plwiki Stwardnienie zanikowe boczne
• ptwiki Esclerose lateral amiotrófica
• rowiki Scleroză laterală amiotrofică
• ruwiki Боковой амиотрофический склероз
• scowiki Motor neurone tribbles
• shwiki Amiotrofična lateralna skleroza
• simplewiki Motor neurone disease
• siwiki පේෂීපෝෂණ පාර්ශ්වීය ජාරඨ්‍යය
• skwiki Amyotrofická laterálna skleróza
• slwiki Amiotrofična lateralna skleroza
• srwiki Amiotrofična lateralna skleroza
• svwiki Amyotrofisk lateralskleros
• swwiki Sklerosisi ya kimiotrofia ya pembezoni
• tawiki தசையூட்டமற்ற பக்க மரப்பு நோய்
• thwiki อะไมโอโทรฟิก แลเทอรัล สเกลอโรซิส
• tlwiki Amyotrophic lateral sclerosis
• trwiki Amyotrofik lateral skleroz
• ukwiki Бічний аміотрофічний склероз
• viwiki Xơ cứng teo cơ một bên
• wuuwiki 肌萎缩性脊髓侧索硬化症
• xmfwiki ამიოტროფული სკლეროზი
• yiwiki ALS
• zh_yuewiki 肌肉萎縮性脊髓側索硬化症
• zhwiki 肌萎缩性脊髓侧索硬化症

Wikibooks(0 entries)

Vicínuacht(1 entry)

• ruwikinews Категория:Боковой амиотрофический склероз

Vicíshliocht(1 entry)

• itwikiquote Sclerosi laterale amiotrofica

Vicífhoinse(0 entries)

Wikiversity(0 entries)

Vicíthaisteal(0 entries)

Wiktionary(0 entries)

Suíomhanna eile(0 entries)

Aisghafa ó "https://www.wikidata.org/w/index.php?title=Q206901&oldid=2149025963"