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Corneal Dystrophies, Hereditary
MeSH HeadingCorneal Dystrophies, Hereditary
Tree NumberC11.204.236
Tree NumberC11.270.162
Tree NumberC16.320.290.162
Scope NoteBilateral hereditary disorders of the cornea, usually autosomal dominant, which may be present at birth but more frequently develop during adolescence and progress slowly throughout life. Central macular dystrophy is transmitted as an autosomal recessive defect.
Entry TermGranular Dystrophy, Corneal
Entry TermGroenouw's Dystrophies
Entry TermMacular Dystrophy, Corneal
Entry TermStromal Dystrophies, Corneal
Allowable QualifiersBL CF CI CL CO DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RA RH RI RT SU TH UR US VE VI
Online Noteuse CORNEAL DYSTROPHIES, HEREDITARY to search CORNEAL DYSTROPHIES 1966-89
History Note90; was CORNEAL DYSTROPHIES 1963-89
Date of Entry19990101
Unique IDD003317


MeSH Tree Structures

 
Eye Diseases [C11]
   Corneal Diseases [C11.204]
Arrow pointing to current tree nodeCorneal Dystrophies, Hereditary [C11.204.236]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C11.204.236.218]
Fuchs' Endothelial Dystrophy [C11.204.236.438]
Corneal Edema [C11.204.267]
Corneal Endothelial Cell Loss [C11.204.278]
Corneal Neovascularization [C11.204.290]
Corneal Opacity [C11.204.299]  +
Corneal Perforation [C11.204.365]
Corneal Wavefront Aberration [C11.204.431]
Iridocorneal Endothelial Syndrome [C11.204.497]
Keratitis [C11.204.564]  +
Keratoconus [C11.204.627]
Trachoma [C11.204.813]

 
Eye Diseases [C11]
   Eye Diseases, Hereditary [C11.270]
Aicardi Syndrome [C11.270.019]
Albinism [C11.270.040]  +
Aniridia [C11.270.060]  +
Choroideremia [C11.270.142]
Arrow pointing to current tree nodeCorneal Dystrophies, Hereditary [C11.270.162]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C11.270.162.218]
Fuchs' Endothelial Dystrophy [C11.270.162.438]
Duane Retraction Syndrome [C11.270.235]
Gyrate Atrophy [C11.270.468]
Leber Congenital Amaurosis [C11.270.516]
Optic Atrophies, Hereditary [C11.270.564]  +
Retinal Dysplasia [C11.270.660]
Retinitis Pigmentosa [C11.270.684]  +
Graves Ophthalmopathy [C11.270.842]
Walker-Warburg Syndrome [C11.270.881]
Weill-Marchesani Syndrome [C11.270.921]

 
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
   Genetic Diseases, Inborn [C16.320]
      Eye Diseases, Hereditary [C16.320.290]
Aicardi Syndrome [C16.320.290.019]
Albinism [C16.320.290.040]  +
Aniridia [C16.320.290.078]  +
Choroideremia [C16.320.290.142]
Arrow pointing to current tree nodeCorneal Dystrophies, Hereditary [C16.320.290.162]
Corneal Dystrophy, Juvenile Epithelial of Meesmann [C16.320.290.162.204]
Fuchs' Endothelial Dystrophy [C16.320.290.162.410]
Duane Retraction Syndrome [C16.320.290.235]
Gyrate Atrophy [C16.320.290.468]
Optic Atrophies, Hereditary [C16.320.290.564]  +
Retinal Dysplasia [C16.320.290.660]
Retinitis Pigmentosa [C16.320.290.684]  +
Vitelliform Macular Dystrophy [C16.320.290.763]
Weill-Marchesani Syndrome [C16.320.290.842]

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