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posterior polymorphous corneal dystrophy 1

http://purl.obolibrary.org/obo/DOID_0110855

A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

posterior polymorphous corneal dystrophy 1

Synonyms

Ched1
Corneal Endothelial Dystrophy 1, Autosomal Dominant
Maumenee Corneal Dystrophy
Ppcd1

database cross reference

has obo namespace

disease_ontology

DOID:0110855

Term relations

Subclass of:

autosomal dominant disease
posterior polymorphous corneal dystrophy
has material basis in some autosomal dominant inheritance