(Q7434154)

English

sclerocornea

corneal disease in which the cornea blends with sclera, resulting in clouding of the cornea

isolated congenital sclerocornea

In more languages

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Statements

0 references

1 reference

30 November 2020

corneogoniodysgenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0019629

clouding of the corneas

0 references

3 references

A Cohesin Subunit Variant Identified from a Peripheral Sclerocornea Pedigree

PubMed ID

31173765

stated in

A sclerocornea-associated RAD21 variant induces corneal stroma disorganization

type of reference

review article

stated in

Cohesin Subunit RAD21: from Biology to Disease

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0060252

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0060252

1 reference

stated in

Identifiers.org

reference URL

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

http://purl.obolibrary.org/obo/HP_0000647

1 reference

stated in

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0000647

http://www.orpha.net/ORDO/Orphanet_91490

0 references

Identifiers

MeSH descriptor ID

C565209

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

2 references

28 August 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

1 reference

30 November 2020

Human Phenotype Ontology ID

HP:0000647

2 references

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

Microsoft Academic ID

0 references

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

28 July 2018

2 references

28 August 2019

Human Phenotype Ontology release 2018-03-08

retrieved

8 October 2018

Human Phenotype Ontology ID

HP:0000647

C5681467

1 reference

based on heuristic

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

Sitelinks

Wikipedia(2 entries)

dewiki Sklerokornea
enwiki Sclerocornea

(Q7434154)

sclerocornea

Statements

Identifiers

Sitelinks

Wikipedia(2 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

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Wiktionary(0 entries)

Multilingual sites(0 entries)