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Metadata
ID DOID:0110855
Name posterior polymorphous corneal dystrophy 1
Definition A posterior polymorphous corneal dystrophy that has_material_basis_in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23.
https://www.ncbi.nlm.nih.gov/pubmed/26749309
Xrefs

ICD10CM:H18.50

MIM:122000

Synonyms

CHED1 [EXACT]

Corneal Endothelial Dystrophy 1, Autosomal Dominant [EXACT]

Maumenee Corneal Dystrophy [EXACT]

PPCD1 [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a posterior polymorphous corneal dystrophy

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

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