Search Ontology:
Human Disease

posterior amorphous corneal dystrophy

Term ID
DOID:0060452
Synonyms
  • chromosome 12q21.33 deletion syndrome
  • PACD
Definition
A stromal dystrophy that is characterized by irregular sheetlike areas of opacification with involvement of the Descemet membrane and, in some instances, alterations of the normal endothelial mosaic and that has_material_basis_in a chromosome 12q21.33 contiguous gene deletion syndrome. https://pubmed.ncbi.nlm.nih.gov/27096414/
References
Ontology
Human Disease   ( DOID:0060452 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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