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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
congenital hereditary endothelial dystrophy of cornea  
CORNEAL DYSTROPHY, PUNCTIFORM AND POLYCHROMATIC PRE-DESCEMET  
Fuchs' endothelial dystrophy +   
A corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision. (DO)
Iridocorneal Endothelial Syndrome +  
X-linked endothelial corneal dystrophy 

Synonyms
Exact Synonyms: FCED ;   Fuch endothelial dystrophy ;   Fuch's endothelial dystrophy ;   Fuchs Corneal Dystrophy ;   Fuchs Dystrophy ;   Fuchs atrophy ;   Fuchs endothelial corneal dystrophy
Primary IDs: MESH:D005642
Xrefs: EFO:0003946 ;   GARD:10018 ;   ICD10CM:H18.51 ;   MIM:PS136800 ;   MONDO:0005321 ;   NCI:C84721 ;   ORDO:98974
Definition Sources: http://en.wikipedia.org/wiki/Fuchs%27_dystrophy "DO" "DO", http://ghr.nlm.nih.gov/condition/fuchs-endothelial-dystrophy "DO" "DO", http://rarediseases.info.nih.gov/gard/10018/corneal-dystrophy-fuchs-endothelial-1/resources/1 "DO" "DO", http://www.mayoclinic.org/diseases-conditions/fuchs-dystrophy/basics/definition/con-20023893?_ga=1.163328703.2017809229.1415219956 "DO" "DO"

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