(Q4976847)

English

Brown-Vialetto-Van Laere syndrome

Human disease

In more languages

Statements

class of disease

0 references

autosomal dominant disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

infantile progressive bulbar palsy

0 references

genetic association

2 references

9 December 2020

https://search.clinicalgenome.org/kb/gene-validity/b0ae82e2-4c39-45b2-ba2d-6fe2570dbcfc--2018-09-18T04:00:00

26 January 2021

https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_b0ae82e2-4c39-45b2-ba2d-6fe2570dbcfc-2018-09-18T040000.000Z

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C133724

0 references

http://purl.obolibrary.org/obo/DOID_0050694

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

http://identifiers.org/doid/DOID:0050694

1 reference

Identifiers.org

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

Identifiers

MeSH descriptor ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

PatientsLikeMe condition ID

0 references

0 references

Disease Ontology ID

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

imported from Wikimedia project

English Wikipedia

Microsoft Academic ID

0 references

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

UniProt disease ID

0 references

WikiProjectMed ID

Brown–Vialetto–Van Laere syndrome

0 references

Sitelinks

Wikipedia(4 entries)

dewiki Brown-Vialetto-van-Laere-Syndrom
enwiki Brown–Vialetto–Van Laere syndrome
iswiki BVVL
plwiki Zespół Browna-Vialetto-Van Laerego

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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