Amiotrofična lateralna skleroza (Q206901)

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rare neurodegenerative disease with amyotrophy and progressive paralysis ^engleski

• ALS

Jezik	Naziv	Opis	Sinonimi
hrvatski	Amiotrofična lateralna skleroza	Opis nije unesen	ALS
engleski	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

Izvadci

jest

designated intractable/rare disease ^engleski

3 referencije

URL referencije

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

preuzeto

6. prosinca 2018

URL referencije

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

preuzeto

6. prosinca 2018

URL referencije

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

preuzeto

17. svibnja 2019

rijetka bolest

0 referencija

class of disease ^engleski

0 referencija

symptom or sign ^engleski

0 referencija

dio klase

motor neuron disease ^engleski

3 referencije

navedeno u

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

navedeno u

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

navedeno u

Disease Ontology ^engleski

preuzeto

30. studenoga 2020

Disease Ontology ID

DOID:332

TDP-43 Proteinopathies ^engleski

0 referencija

neurodegeneration ^engleski

1 referencija

navedeno u

Monarch Disease Ontology release 2018-06-29 ^engleski

preuzeto

3. srpnja 2018

Mondo ID ^engleski

MONDO_0004976

monogenic disease ^engleski

1 referencija

navedeno u

Disease Ontology ^engleski

preuzeto

30. studenoga 2020

Disease Ontology ID

DOID:332

bolest

0 referencija

slika

ALS Coronal.jpg
920 × 938; 102 KB

1 referencija

uvezeno iz

Wikipedija na ruskom jeziku

nadimak

Lou Gehrig's disease (engleski)

1 referencija

URL referencije

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

skraćeno ime

ELA (katalonski)

0 referencija

ALS (engleski)

0 referencija

zvučni zapis izgovora

LL-Q33810 (ori)-Psubhashish-ଆମାୟୋଟ୍ରୋଫିକ୍ ଲାଟେରାଲ ସ୍କ୍ଲେରୋସିସ୍.wav
3,3 s; 307 KB

jezik djela ili imena

oriya jezici

1 referencija

URL referencije

https://lingualibre.org/wiki/Q648173

nazvano po

Lou Gehrig ^engleski

0 referencija

Jean-Martin Charcot

0 referencija

zahvaća

Motorički neuroni

0 referencija

health specialty ^engleski

neurologija

0 referencija

medicinske pretrage

Awaji Criteria ^engleski

0 referencija

drug or therapy used for treatment ^engleski

riluzole ^engleski

2 referencije

navedeno u

NDF-RT ^engleski

NDF-RT ID ^engleski

N0000148421

jezik djela ili imena

engleski

preuzeto

13. prosinca 2016

navedeno u

Drug Indications Extracted from FAERS ^engleski

preuzeto

2. listopada 2018

edaravone ^engleski

1 referencija

navedeno u

Drug Indications Extracted from FAERS ^engleski

preuzeto

2. listopada 2018

riluzole ^engleski

vrijeme početka

12. prosinca 1995

approved by ^engleski

Food and Drug Administration ^engleski

1 referencija

navedeno u

Inxight: Drugs Database ^engleski

preuzeto

2. studenoga 2018

URL referencije

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

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

edaravone ^engleski

vrijeme početka

14. siječnja 2010

approved by ^engleski

Food and Drug Administration ^engleski

1 referencija

navedeno u

Inxight: Drugs Database ^engleski

preuzeto

2. studenoga 2018

URL referencije

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

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

genetic association ^engleski

ITGA9 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CTNND2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

TSPAN9 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

TFAP2A ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ATP2B2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

EPB41 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

LRRC8C ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

NFASC ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

SLC25A12 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ERBB4 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

14. ožujka 2020

TRPM8 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

KCNMB2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

MASP1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ANXA3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

SYNPO2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

INPP4B ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

LAMA2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CALN1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

TBXAS1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

PDGFRL ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ANK3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

LDHC ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

RBM19 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

TMEM132B ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

OLFM4 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

DACH1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ZFYVE26 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

RGS6 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ABCC12 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

NEDD4L ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

MACROD2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

PROCR ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

NFATC2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CHODL ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

HOXD10 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

MRAS ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ABCG1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ANKRD29 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

UNC13A ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CPNE4 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

KIAA0513 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

LAMA3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ST3GAL3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ARHGEF2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

PTPRF ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ARAP2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

IFRD1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

PCSK5 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CNOT2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ANKS1B ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

18. veljače 2020

NRXN3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

B4GALT6 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

NT5C1A ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

SLC39A11 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ATXN1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

CNTN4 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

KIFAP3 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

SELL ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

DPP6 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ITPR2 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

ZFP64 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

SUSD1 ^engleski

način određivanja

genome-wide association study ^engleski

TAS ^engleski

1 referencija

URL referencije

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

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

navedeno u

Phenocarta ^engleski

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

preuzeto

25. svibnja 2020

NEK1 ^engleski

1 referencija

DOI ^engleski

10.1038/NG.3626

SQSTM1 ^engleski

1 referencija

navedeno u

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis ^engleski

ANG ^engleski

1 referencija

navedeno u

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

TARDBP ^engleski

3 referencije

navedeno u

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

navedeno u

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

navedeno u

Open Targets Platform ^engleski

preuzeto

24. kolovoza 2023

URL referencije

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

based on heuristic ^engleski

inferred from an Open Targets association score over 0.7 ^engleski

TUBA4A ^engleski

1 referencija

navedeno u

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

FIG4 ^engleski

2 referencije

navedeno u

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

navedeno u

Open Targets Platform ^engleski

preuzeto

24. kolovoza 2023

URL referencije

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

based on heuristic ^engleski

inferred from an Open Targets association score over 0.7 ^engleski

OPTN ^engleski

2 referencije

navedeno u

Mutations of optineurin in amyotrophic lateral sclerosis ^engleski

navedeno u

Open Targets Platform ^engleski

preuzeto

24. kolovoza 2023

URL referencije

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

based on heuristic ^engleski

inferred from an Open Targets association score over 0.7 ^engleski

FUS ^engleski

1 referencija

navedeno u

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

SOD1 ^engleski

2 referencije

navedeno u

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

navedeno u

Open Targets Platform ^engleski

preuzeto

24. kolovoza 2023

URL referencije

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

based on heuristic ^engleski

inferred from an Open Targets association score over 0.7 ^engleski

VCP ^engleski

2 referencije

navedeno u

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

navedeno u

Open Targets Platform ^engleski

preuzeto

24. kolovoza 2023

URL referencije

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

based on heuristic ^engleski

inferred from an Open Targets association score over 0.7 ^engleski

HNRNPA1 ^engleski

1 referencija

navedeno u

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

PFN1 ^engleski

1 referencija

navedeno u

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

UBQLN2 ^engleski

1 referencija

navedeno u

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

VAPB ^engleski

1 referencija

navedeno u

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

CHMP2B ^engleski

1 referencija

navedeno u

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

external data available at URL ^engleski

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

jezik djela ili imena

japanski jezik

1 referencija

URL referencije

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

preuzeto

17. svibnja 2019

on focus list of Wikimedia project ^engleski

Wikipedija:Wikiprojekt medicina

0 referencija

MKB-9-CM

335.20

2 referencije

navedeno u

Disease Ontology ^engleski

preuzeto

15. svibnja 2019

Disease Ontology ID

DOID:332

navedeno u

Monarch Disease Ontology release 2018-06-29 ^engleski

preuzeto

3. srpnja 2018

Mondo ID ^engleski

MONDO_0004976

ICPC 2

N99

1 referencija

uvezeno iz

Wikipedija na španjolskom jeziku

NCI Thesaurus ID

C34373

1 referencija

navedeno u

Disease Ontology ^engleski

preuzeto

15. svibnja 2019

Disease Ontology ID

DOID:332

exact match ^engleski

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

1 referencija

navedeno u

Disease Ontology ^engleski

preuzeto

30. studenoga 2020

Disease Ontology ID

DOID:332

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

1 referencija

navedeno u

Identifiers.org ^engleski

URL referencije

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

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

1 referencija

navedeno u

Human Phenotype Ontology release 2018-03-08 ^engleski

preuzeto

8. listopada 2018

Human Phenotype Ontology ID ^engleski

HP:0007354

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

0 referencija

kategorija na Zajedničkom poslužitelju

Amyotrophic lateral sclerosis

0 referencija

glavni predložak teme

Template:Amyotrophic lateral sclerosis ^engleski

1 referencija

inferred from ^engleski

Template:Amyotrophic lateral sclerosis ^engleski

glavna kategorija teme

Category:Amyotrophic lateral sclerosis ^engleski

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

Identifikatori

BNF

12110754p

0 referencija

National Library of Israel J9U ID ^engleski

987007294733105171

1 referencija

navedeno u

National Library of Israel ^engleski

LCCN

sh85004728

0 referencija

National Library of Latvia ID ^engleski

000125199

0 referencija

NDL ID

01127913

0 referencija

NKCR broj

ph397748

naveden kao

amyotrofická laterální skleróza

0 referencija

MeSH ID

D000690

mapping relation type ^engleski

exact match ^engleski

naveden kao

Amyotrophic Lateral Sclerosis

1 referencija

navedeno u

Monarch Disease Ontology release 2018-06-29 ^engleski

preuzeto

3. srpnja 2018

Mondo ID ^engleski

MONDO_0004976

MeSH

C10.228.854.139

0 referencija

C10.574.562.250

0 referencija

C10.574.950.050

0 referencija

C10.668.467.250

0 referencija

C18.452.845.800.050

0 referencija

MedlinePlus ID

000688

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

PatientsLikeMe condition ID ^engleski

als

0 referencija

KEGG ID ^engleski

H00058

0 referencija

AniDB tag ID ^engleski

847

0 referencija

BBC Things ID ^engleski

6c2f0633-2664-4233-ba56-5ce53cb764f9

1 referencija

navedeno u

BBC Things ^engleski

BNCF Thesaurus ID

36605

1 referencija

navedeno u

National Central Library of Florence ^engleski

Disease Ontology ID

DOID:332

1 referencija

navedeno u

Disease Ontology ^engleski

preuzeto

30. studenoga 2020

Disease Ontology ID

DOID:332

DiseasesDB ID

29148

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

eMedicine ID

1170097

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

791154

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

306543

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

Freebase ID

/m/017s1k

1 referencija

navedeno u

Freebase Data Dumps ^engleski

datum izdavanja

28. listopada 2013

French Vikidia ID ^engleski

Maladie_de_Charcot

0 referencija

GARD rare disease ID ^engleski

5786

0 referencija

Genetics Home Reference Conditions ID ^engleski

amyotrophic-lateral-sclerosis

0 referencija

Gran Enciclopèdia Catalana ID ^engleski

esclerosi-lateral

0 referencija

Gran Enciclopèdia Catalana ID (former scheme) ^engleski

0180358

0 referencija

Great Russian Encyclopedia Online ID (old version) ^engleski

4424982

naveden kao

АМИОТРОФИЧЕСКИЙ БОКОВОЙ СКЛЕРОЗ

0 referencija

1818344

reason for deprecated rank ^engleski

redirect ^engleski

0 referencija

Human Phenotype Ontology ID ^engleski

HP:0007354

1 referencija

navedeno u

Human Phenotype Ontology release 2018-03-08 ^engleski

preuzeto

8. listopada 2018

Human Phenotype Ontology ID ^engleski

HP:0007354

ICD-10-CM ^engleski

G12.21

2 referencije

navedeno u

Disease Ontology ^engleski

preuzeto

15. svibnja 2019

Disease Ontology ID

DOID:332

navedeno u

Monarch Disease Ontology release 2018-06-29 ^engleski

preuzeto

3. srpnja 2018

Mondo ID ^engleski

MONDO_0004976

G12.2

1 referencija

navedeno u

Monarch Disease Ontology release 2018-06-29 ^engleski

preuzeto

3. srpnja 2018

Mondo ID ^engleski

MONDO_0004976

ICD-11 (foundation) ^engleski

1982355687

0 referencija

ICD-11 ID (MMS) ^engleski

8B60.0

naveden kao

Amyotrophic lateral sclerosis

0 referencija

MKB-9

335.20

1 referencija

uvezeno iz

Wikipedija na ruskom jeziku

URL uvoza s Wikimedije

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

internetmedicin.se ID ^engleski

1054

1 referencija

uvezeno iz

Wikipedija na švedskom jeziku

JSTOR topic ID ^engleski

amyotrophic-lateral-sclerosis

0 referencija

KBpedia ID ^engleski

AmyotrophicLateralSclerosis

1 referencija

navedeno u

KBpedia ^engleski

preuzeto

9. srpnja 2020

Le Figaro tag ID ^engleski

maladie-de-Charcot

0 referencija

Mondo ID ^engleski

MONDO_0004976

0 referencija

OMIM ID

105400

1 referencija

uvezeno iz

Wikipedija na engleskom jeziku

URL uvoza s Wikimedije

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

OpenAlex ID ^engleski

C2778466831

1 referencija

navedeno u

OpenAlex ^engleski

preuzeto

26. siječnja 2022

URL referencije

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

C2780596555

1 referencija

navedeno u

OpenAlex ^engleski

preuzeto

26. siječnja 2022

URL referencije

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

Orphanet ID

803

1 referencija

navedeno u

Disease Ontology ^engleski

preuzeto

15. svibnja 2019

Disease Ontology ID

DOID:332

Patientplus ID

Motor-Neurone-Disease-(MND)

1 referencija

URL referencije

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

ID oznaka teme na Quori

Amyotrophic-Lateral-Sclerosis-ALS

0 referencija

Store medisinske leksikon ID ^engleski

ALS_-_amyotrofisk_lateral_sklerose

0 referencija

subreddit ^engleski

ALS

1 referencija

URL referencije

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

naslov

ALS (engleski)

preuzeto

28. studenoga 2021

UK Parliament thesaurus ID ^engleski

288352

naveden kao

Motor neurone disease

0 referencija

UMLS CUI ^engleski

C0002736

2 referencije

navedeno u

Disease Ontology ^engleski

preuzeto

15. svibnja 2019

Disease Ontology ID

DOID:332

navedeno u

Human Phenotype Ontology release 2018-03-08 ^engleski

preuzeto

8. listopada 2018

Human Phenotype Ontology ID ^engleski

HP:0007354

C0393554

1 referencija

based on heuristic ^engleski

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

navedeno u

UMLS 2023 ^engleski

preuzeto

25. svibnja 2023

UniProt disease ID ^engleski

DI-00107

0 referencija

WikiKids ID ^engleski

Amyotrofe_laterale_sclerose

0 referencija

WikiProjectMed ID ^engleski

Amyotrophic lateral sclerosis

0 referencija

WikiSkripta article ID ^engleski

31784

0 referencija

YSO ID ^engleski

8108

1 referencija

navedeno u

YSO-Wikidata mapping project ^engleski

 

Poveznice na mrežna mjesta

Wikipedija(68 unosa)

• 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

Wikiknjige(0 unosa)

Wijesti(1 unos)

• ruwikinews Категория:Боковой амиотрофический склероз

Wikicitat(1 unos)

• itwikiquote Sclerosi laterale amiotrofica

Wikizvor(0 unosa)

Wikiučilište(0 unosa)

Wikiputovanja(0 unosa)

Wječnik(0 unosa)

Druge lokacije(0 unosa)

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