Search Ontology:
Human Disease

posterior polymorphous corneal dystrophy 1

Term ID
DOID:0110855
Synonyms
  • CHED1
  • Corneal Endothelial Dystrophy 1, Autosomal Dominant
  • Maumenee Corneal Dystrophy
  • PPCD1
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
References
Ontology
Human Disease   ( DOID:0110855 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models