(Q4183965)

English

posterior polymorphous corneal dystrophy

Human disease

PPCD
Schlichting dystrophy
hereditary polymorphus posterior corneal dystrophy
Posterior polymorphous dystrophy

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Statements

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corneal endothelial dystrophy

1 reference

15 May 2019

1 reference

30 November 2020

1 reference

Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells

COL8A2

1 reference

stated in

Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy

on focus list of Wikimedia project

WikiProject Medicine

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exact match

http://purl.obolibrary.org/obo/DOID_0060457

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0060457

1 reference

stated in

Identifiers.org

reference URL

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

http://purl.obolibrary.org/obo/HP_0007915

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0007915

http://www.orpha.net/ORDO/Orphanet_98973

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Commons category

Posterior polymorphous corneal dystrophy

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Identifiers

2 references

28 August 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0007915

C562745

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

7 August 2018

Mondo ID

MONDO_0020364

PatientsLikeMe condition ID

polymorphous-corneal-dystrophy

0 references

0 references

1 reference

30 November 2020

Human Phenotype Ontology ID

HP:0007915

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

2 references

28 August 2019

Monarch Disease Ontology release 2018-06-29

7 August 2018

0 references

Microsoft Academic ID

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1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

7 August 2018

1 reference

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0007915

C1852555

1 reference

based on heuristic

inferred by common MeSH mappings on source and on Wikidata

25 May 2023

Posterior polymorphous corneal dystrophy

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Sitelinks

Wikipedia(3 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Posterior polymorphous corneal dystrophy