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CRYGD

MIM.123690 2q33-q35

Pathology

- germline mutations in

  • juvenile-onset progressive punctate cataract (autosomal dominant punctate cataract of early postnatal onset and progressive nature)
  • aculeiform cataract (MIM.115700)
  • congenital lamellar cataract
  • congenital cerulean cataract type 3 (MIM.608983)
  • autosomal dominant nonnuclear congenital polymorphic cataract (MIM.601286)

See also

- CRYs

  • CRYGs