(Q4127191)

English

congenital hereditary endothelial dystrophy of cornea

Human disease

  • CHED
  • Maumenee Corneal Dystrophy
  • CORNEAL ENDOTHELIAL DYSTROPHY 2, AUTOSOMAL RECESSIVE; CHED2
  • CORNEAL ENDOTHELIAL DYSTROPHY 2, AUTOSOMAL RECESSIVE
  • Corneal Dystrophy, Congenital Hereditary Endothelial
  • Congenital hereditary endothelial dystrophy type 2
  • CHED2, FORMERLY
  • CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY OF CORNEA
  • CORNEAL ENDOTHELIAL DYSTROPHY 2, AUTOSOMAL RECESSIVE, FORMERLY
  • CORNEAL ENDOTHELIAL DYSTROPHY
  • Infantile hereditary endothelial dystrophy
  • Corneal Endothelial Dystrophy 2
  • Autosomal recessive CHED
  • CHED2
  • CHEDII
  • Corneal endothelial dystrophy type 2
  • Congenital hereditary endothelial dystrophy of the cornea
  • Congenital hereditary endothelial dystrophy type II
  • Autosomal recessive congenital hereditary endothelial dystrophy

Statements

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Congenital hereditary endothelial dystrophy
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Identifiers