(Q18553728)

English

amyotrophic lateral sclerosis type 20

amyotrophic lateral sclerosis with juvenile onset that has material basis in mutation in the HNRNPA1 gene on chromosome 12

ALS20
amyotrophic lateral sclerosis 20
Amyotrophic Lateral Sclerosis type 20
AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20

In more languages

Statements

class of disease

0 references

amyotrophic lateral sclerosis

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

familial amyotrophic lateral sclerosis

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

genetic association

1 reference

UniProt protein ID

13 August 2019

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0060211

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0060211

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233

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

0 references

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

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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