Амиотрофична латерална склероза (Q206901)

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

6 декември 2018

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

6 декември 2018

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

17 мај 2019

ретка болест

0 наводи

class of disease ^{англиски}

0 наводи

symptom or sign ^{англиски}

0 наводи

поткласа на

motor neuron disease ^{англиски}

3 наводи

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

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

Disease Ontology ^{англиски}

30 ноември 2020

TDP-43 Proteinopathies ^{англиски}

0 наводи

Невродегенерација

1 навод

Monarch Disease Ontology release 2018-06-29 ^{англиски}

3 јули 2018

назнака на Mondo

MONDO_0004976

monogenic disease ^{англиски}

1 навод

Disease Ontology ^{англиски}

30 ноември 2020

болест

0 наводи

фотографија

ALS Coronal.jpg
920 × 938; 102 КБ

1 навод

Википедија на руски јазик

прекар

Lou Gehrig's disease (англиски)

1 навод

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

краток назив

ELA (каталонски)

0 наводи

ALS (англиски)

0 наводи

изговор (звуч. запис)

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

јазик на делото/името

одиски јазик

1 навод

https://lingualibre.org/wiki/Q648173

наречено по

Лу Гериг

0 наводи

Jean-Martin Charcot ^{англиски}

0 наводи

погодува

motor neuron ^{англиски}

0 наводи

медицинска специјалност

неврологија

0 наводи

медицински прегледи

Awaji Criteria ^{англиски}

0 наводи

се користи лекот

riluzole ^{англиски}

2 наводи

NDF-RT ^{англиски}

назнака на NDF-RT

N0000148421

јазик на делото/името

англиски јазик

13 декември 2016

Drug Indications Extracted from FAERS ^{англиски}

2 октомври 2018

edaravone ^{англиски}

1 навод

Drug Indications Extracted from FAERS ^{англиски}

2 октомври 2018

riluzole ^{англиски}

почетен датум

12 декември 1995

одобрил

Управа за храна и лекови

1 навод

Inxight: Drugs Database ^{англиски}

2 ноември 2018

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

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

edaravone ^{англиски}

почетен датум

14 јануари 2010

одобрил

Управа за храна и лекови

1 навод

Inxight: Drugs Database ^{англиски}

2 ноември 2018

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

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

генетска врска

ITGA9 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CTNND2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

TSPAN9 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

TFAP2A ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ATP2B2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

EPB41 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

LRRC8C ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

NFASC ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

SLC25A12 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ERBB4 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

14 март 2020

TRPM8 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

KCNMB2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

MASP1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ANXA3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

SYNPO2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

INPP4B ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

LAMA2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CALN1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

TBXAS1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

PDGFRL ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ANK3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

LDHC ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

RBM19 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

TMEM132B ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

OLFM4 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

DACH1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ZFYVE26 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

RGS6 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ABCC12 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

NEDD4L ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

MACROD2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

PROCR ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

NFATC2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CHODL ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

HOXD10 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

MRAS ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ABCG1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ANKRD29 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

UNC13A ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CPNE4 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

KIAA0513 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

LAMA3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ST3GAL3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ARHGEF2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

PTPRF ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ARAP2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

IFRD1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

PCSK5 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CNOT2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ANKS1B ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

18 февруари 2020

NRXN3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

B4GALT6 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

NT5C1A ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

SLC39A11 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ATXN1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

CNTN4 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

KIFAP3 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

SELL ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

DPP6 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

Screening for replication of genome-wide SNP associations in sporadic ALS ^{англиски}

25 мај 2020

ITPR2 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

ZFP64 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

SUSD1 ^{англиски}

genome-wide association study ^{англиски}

TAS ^{англиски}

1 навод

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

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

Phenocarta ^{англиски}

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

25 мај 2020

NEK1 ^{англиски}

1 навод

DOI

10.1038/NG.3626

SQSTM1 ^{англиски}

1 навод

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis ^{англиски}

ANG ^{англиски}

1 навод

A novel candidate region for ALS on chromosome 14q11.2. ^{англиски}

TARDBP ^{англиски}

3 наводи

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

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis ^{англиски}

Open Targets Platform ^{англиски}

24 август 2023

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

inferred from an Open Targets association score over 0.7 ^{англиски}

TUBA4A ^{англиски}

1 навод

Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. ^{англиски}

FIG4 ^{англиски}

2 наводи

Deleterious variants of FIG4, a phosphoinositide phosphatase, in patients with ALS. ^{англиски}

Open Targets Platform ^{англиски}

24 август 2023

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

inferred from an Open Targets association score over 0.7 ^{англиски}

OPTN ^{англиски}

2 наводи

Mutations of optineurin in amyotrophic lateral sclerosis ^{англиски}

Open Targets Platform ^{англиски}

24 август 2023

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

inferred from an Open Targets association score over 0.7 ^{англиски}

FUS ^{англиски}

1 навод

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

SOD1 ^{англиски}

2 наводи

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

Open Targets Platform ^{англиски}

24 август 2023

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

inferred from an Open Targets association score over 0.7 ^{англиски}

VCP ^{англиски}

2 наводи

Exome sequencing reveals VCP mutations as a cause of familial ALS ^{англиски}

Open Targets Platform ^{англиски}

24 август 2023

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

inferred from an Open Targets association score over 0.7 ^{англиски}

HNRNPA1 ^{англиски}

1 навод

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS ^{англиски}

PFN1 ^{англиски}

1 навод

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis ^{англиски}

UBQLN2 ^{англиски}

1 навод

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

VAPB ^{англиски}

1 навод

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

CHMP2B ^{англиски}

1 навод

извор на надворешни податоци

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B) ^{англиски}

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

јазик на делото/името

јапонски јазик

1 навод

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

на работен список на Викимедиин проект

17 мај 2019

Википедија:ВикиПроект Медицина

0 наводи

МКБ-9-КП

335.20

2 наводи

Disease Ontology ^{англиски}

15 мај 2019

Monarch Disease Ontology release 2018-06-29 ^{англиски}

3 јули 2018

N99

1 навод

Википедија на шпански јазик

назнака во толковникот на NCI

C34373

1 навод

Disease Ontology ^{англиски}

15 мај 2019

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

точно совпаѓање

1 навод

Disease Ontology ^{англиски}

30 ноември 2020

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

1 навод

Identifiers.org

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

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

1 навод

Human Phenotype Ontology release 2018-03-08 ^{англиски}

8 октомври 2018

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

HP:0007354

0 наводи

категорија на Ризницата

Amyotrophic lateral sclerosis

0 наводи

главна тематска предлошка

Template:Amyotrophic lateral sclerosis ^{англиски}

1 навод

заклучено според

Template:Amyotrophic lateral sclerosis ^{англиски}

главна категорија на статијата

Category:Amyotrophic lateral sclerosis ^{англиски}

1 навод

Израелска национална библиотека

Назнаки

0 наводи

1 навод

0 наводи

0 наводи

0 наводи

amyotrofická laterální skleróza

0 наводи

MeSH-назнака

D000690

вид однос на пресликувањето

точно совпаѓање

наведен како

Amyotrophic Lateral Sclerosis

1 навод

Monarch Disease Ontology release 2018-06-29 ^{англиски}

3 јули 2018

0 наводи

0 наводи

0 наводи

0 наводи

0 наводи

1 навод

6c2f0633-2664-4233-ba56-5ce53cb764f9

PatientsLikeMe condition ID ^{англиски}

0 наводи

0 наводи

0 наводи

назнака на BBC Things

1 навод

1 навод

Национална централна библиотека на Фиренца

1 навод

Disease Ontology ^{англиски}

30 ноември 2020

1 навод

eMedicine

1170097

1 навод

791154

1 навод

306543

1 навод

назнака на Freebase

/m/017s1k

1 навод

базна резерва на Freebase

датум на издавање

28 октомври 2013

на француската Викидија

Maladie_de_Charcot

0 наводи

GARD rare disease ID ^{англиски}

5786

0 наводи

Genetics Home Reference Conditions ID ^{англиски}

amyotrophic-lateral-sclerosis

0 наводи

Gran Enciclopèdia Catalana ID ^{англиски}

esclerosi-lateral

0 наводи

назнака во Големата каталонска енциклопедија

0180358

0 наводи

назнака на семрежната Голема руска енциклопедија

4424982

наведен како

АМИОТРОФИЧЕСКИЙ БОКОВОЙ СКЛЕРОЗ

0 наводи

1818344

причина за застареноста

пренасочување

0 наводи

HP:0007354

1 навод

Human Phenotype Ontology release 2018-03-08 ^{англиски}

8 октомври 2018

2 наводи

Disease Ontology ^{англиски}

15 мај 2019

Monarch Disease Ontology release 2018-06-29 ^{англиски}

3 јули 2018

1 навод

Monarch Disease Ontology release 2018-06-29 ^{англиски}

3 јули 2018

0 наводи

8B60.0

Amyotrophic lateral sclerosis

0 наводи

МКБ-9

335.20

1 навод

Википедија на руски јазик

увозна URL од Викимедија

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

назнака на internetmedicin.se ID

1054

1 навод

Википедија на шведски јазик

тематска назнака на JSTOR

amyotrophic-lateral-sclerosis

0 наводи

на KBpedia

AmyotrophicLateralSclerosis

1 навод

KBpedia ^{англиски}

9 јули 2020

Le Figaro tag ID ^{англиски}

0 наводи

0 наводи

1 навод

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

увозна URL од Викимедија

1 навод

OpenAlex ^{англиски}

26 јануари 2022

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

1 навод

OpenAlex ^{англиски}

26 јануари 2022

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

Orphanet-ознака

803

1 навод

Disease Ontology ^{англиски}

15 мај 2019

Motor-Neurone-Disease-(MND)

Patientplus-назнака

1 навод

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

тема на Квора

Amyotrophic-Lateral-Sclerosis-ALS

0 наводи

назнака во норвешкиот Голем медицински лексикон

ALS_-_amyotrofisk_lateral_sklerose

0 наводи

подредит

ALS

1 навод

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

наслов

ALS (англиски)

во Британскиот парламентарен прирачник

28 ноември 2021

288352

наведен како

Motor neurone disease

0 наводи

UMLS CUI

C0002736

2 наводи

Disease Ontology ^{англиски}

15 мај 2019

Human Phenotype Ontology release 2018-03-08 ^{англиски}

8 октомври 2018

HP:0007354

C0393554

1 навод

inferred by common MeSH mappings on source and on Wikidata ^{англиски}

UMLS 2023 ^{англиски}