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2009 ICD-9-CM
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Degeneration, degenerative | |
heredofamilial | |
brain NEC 331.89 | |
spinal cord NEC 336.8 | |
hyaline (diffuse) (generalized) 728.9 | |
localized - see also Degeneration, by site | |
cornea 371.41 | |
keratitis 371.41 | |
hypertensive vascular - see Hypertension | |
infrapatellar fat pad 729.31 | |
internal semilunar cartilage 717.3 | |
intervertebral disc 722.6 | |
with myelopathy 722.70 | |
cervical, cervicothoracic 722.4 | |
with myelopathy 722.71 | |
lumbar, lumbosacral 722.52 | |
with myelopathy 722.73 | |
thoracic, thoracolumbar 722.51 | |
with myelopathy 722.72 | |
intestine 569.89 | |
amyloid 277.39 | |
lardaceous 277.39 | |
iris (generalized) (see also Atrophy, iris) 364.59 | |
pigmentary 364.53 | |
pupillary margin 364.54 | |
ischemic - see Ischemia | |
joint disease (see also Osteoarthrosis) 715.9 | |
multiple sites 715.09 | |
spine (see also Spondylosis) 721.90 | |
kidney (see also Sclerosis, renal) 587 | |
amyloid 277.39 [583.81] | |
cyst, cystic (multiple) (solitary) 593.2 | |
congenital (see also Cystic, disease, kidney) 753.10 | |
fatty 593.89 | |
fibrocystic (congenital) 753.19 | |
lardaceous 277.39 [583.81] | |
polycystic (congenital) 753.12 | |
adult type (APKD) 753.13 | |
autosomal dominant 753.13 | |
autosomal recessive 753.14 | |
childhood type (CPKD) 753.14 | |
infantile type 753.14 | |
waxy 277.39 [583.81] | |
kuhnt-Junius (retina) 362.52 | |
labyrinth, osseous 386.8 | |
lacrimal passages, cystic 375.12 | |
lardaceous (any site) 277.39 | |
lateral column (posterior), spinal cord (see also Degeneration, combined) 266.2 [336.2] | |
lattice 362.63 | |
lens 366.9 | |
infantile, juvenile, or presenile 366.00 | |