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corneal dystrophy, lattice type 1An autosomal dominant (OMIM:122200) form of corneal dystrophy characterised by wispy, greyish, cotton-like threads limited to a zone between the centre of the cornea and the periphery, with slowly progressive loss of vision by the fifth or sixth decade of life.
Has been linked to defects of TGFBI, which encodes an RGD protein that binds to type I, II and IV collagens and plays a role in cell–collagen interactions.
Segen's Medical Dictionary. © 2012 Farlex, Inc. All rights reserved.
LCDLiquid crystal display Computers A flat panel display used for laptops, PDAs/handhelds, etc. See Laptop computer.
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.
Abbreviation for local coverage determination.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012