CGD2 | definition of CGD2 by Medical dictionary
Avellino corneal dystrophy (redirected from CGD2)
Avellino corneal dystrophy An autosomal dominant (OMIM:607541) form of corneal dystrophy that is considered a variant of granular dystrophy and has a significant amyloidogenic tendency.
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.
References in periodicals archive
Pulmonary and cerebral aspergillosis is an important cause of morbidity and mortality in CGD2
. In low-income countries like ours with endemic tuberculosis (TB), physicians empirically treat patients without microbiological confirmation of TB.
. For each chromosome, we scan from left to right all the edges encoded within it, calculate the index for each edge scanned, and increment the value of the corresponding array element by one.
After the training, average absolute error achieved from the 4 networks; named as QP1 and QP2 for the 2 networks trained in QP and as CGD1 and CGD2
for the networks trained in CGD; are 0.08, 0.09, 0.07 and 0.08, respectively.