(Q18553726)

English

amyotrophic lateral sclerosis type 18

amyotrophic lateral sclerosis that has material basis in mutation in the PFN1 gene on chromosome 17

ALS18
amyotrophic lateral sclerosis 18
Amyotrophic Lateral Sclerosis type 18
AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18

In more languages

Statements

class of disease

0 references

amyotrophic lateral sclerosis

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

familial amyotrophic lateral sclerosis

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

genetic association

3 references

UniProt protein ID

13 August 2019

19 May 2022

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_948de40f-2cef-4235-ae87-491c01ffe803-2021-04-22T160000.000Z

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000108518/MONDO_0013891

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0060209

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0060209

1 reference

Identifiers.org

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

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

0 references

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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