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Congenital hereditary endothelial dystrophy type II

ORPHA:293603 · Disease · Disorder

HPO 表現型（共 9 項）

Very frequent (99-80%)(4)

  • Abnormal Descemet membrane morphologyHP:0011490
  • Corneal opacityHP:0007957
  • Corneal stromal edemaHP:0012040
  • Increased corneal thicknessHP:0011487

Frequent (79-30%)(2)

  • Blurred visionHP:0000622
  • Reduced visual acuityHP:0007663

Occasional (29-5%)(3)

  • Irregular astigmatismHP:0031792
  • NystagmusHP:0000639
  • Sensorineural hearing impairmentHP:0000407