Search Ontology:
Human Disease

Meesmann corneal dystrophy

Term ID
DOID:0060451
Synonyms
  • juvenile hereditary epithelial dystrophy
  • MECD
  • Stocker-Holt dystrophy
Definition
An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium. https://ghr.nlm.nih.gov/condition/meesmann-corneal-dystrophy
References
  • GARD:9688
  • ICD10CM:H18.52
  • ICD9CM:371.51
  • MESH:D053559
  • MIM:PS122100
  • NCI:C84795
  • ORDO:98954
  • SNOMEDCT_US_2023_03_01:193833008
  • UMLS_CUI:C0339277
Ontology
Human Disease   ( DOID:0060451 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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