(Q4127190)

English

congenital hereditary endothelial dystrophy type I

No description defined

CHED1
CHEDI
Congenital hereditary endothelial dystrophy type 1
Autosomal dominant CHED
Autosomal dominant congenital hereditary endothelial dystrophy

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Statements

instance of

class of disease

0 references

subclass of

posterior corneal dystrophy

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

28 July 2018

Mondo ID

MONDO_0020365

congenital hereditary endothelial dystrophy of cornea

0 references

image

Congenital hereditary endothelial dystrophy 1.JPEG
501 × 500; 81 KB

0 references

exact match

http://www.orpha.net/ORDO/Orphanet_98975

0 references

said to be the same as

posterior polymorphous corneal dystrophy 1

1 reference

reference URL

https://pubmed.ncbi.nlm.nih.gov/25564336/

Identifiers

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

Sitelinks

Wikipedia(1 entry)

ruwiki Врождённая эндотелиальная дистрофия роговицы, тип 1

(Q4127190)

congenital hereditary endothelial dystrophy type I

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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