(Q2195280)

English

pontocerebellar hypoplasia type 2A

human disease

PONTOCEREBELLAR HYPOPLASIA, TYPE 2A
Volendam Neurodegenerative Disease
PCH2A
Microcephaly pontocerebellar hypoplasia dyskinesia
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A
Pontocerebellar Hypoplasia With Progressive Cerebral Atrophy
Pch2

In more languages

edit

Statements

0 references

0 references

non-syndromic pontocerebellar hypoplasia

1 reference

29 November 2020

pontocerebellar hypoplasia type 2

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

2 references

13 August 2019

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0060267

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0060267

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_2524

0 references

Identifiers

MeSH descriptor ID

C564738

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

1 reference

29 November 2020

1 reference

28 August 2019

2 references

Monarch Disease Ontology release 2018-06-29

3 July 2018

28 August 2019

Google Knowledge Graph ID

0 references

0 references

1 reference

28 August 2019

1 reference

28 August 2019

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

28 August 2019

0 references

Sitelinks

Wikipedia(1 entry)

nlwiki Pontocerebellaire hypoplasie type 2

(Q2195280)

pontocerebellar hypoplasia type 2A

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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)