Degeneration, degenerative
adrenal
(capsule) (fatty) (gland) (hyaline) (infectional)
E27.8
amyloid
E85.9
Amyloidosis
anterior cornua, spinal cord
G12.29
anterior labral
S43.49-
aorta, aortic
I70.0
fatty
I77.89
aortic valve
(heart)
Endocarditis, aortic
arteriovascular
Arteriosclerosis
artery, arterial
(atheromatous) (calcareous)
Arteriosclerosis
cerebral, amyloid
E85.4
I68.0
medial
Arteriosclerosis, extremities
articular cartilage NEC
Derangement, joint, articular cartilage, by site
atheromatous
Arteriosclerosis
basal nuclei or ganglia
G23.9
specified NEC
G23.8
bone NEC
Disorder, bone, specified type NEC
brachial plexus
G54.0
brain
(cortical) (progressive)
G31.9
alcoholic
G31.2
arteriosclerotic
I67.2
childhood
G31.9
specified NEC
G31.89
cystic
G31.89
congenital
Q04.6
in
alcoholism
G31.2
beriberi
E51.2
cerebrovascular disease
I67.9
congenital hydrocephalus
Q03.9
with spina bifida
Spina bifida
Fabry-Anderson disease
E75.21
Gaucher's disease
E75.22
Hunter's syndrome
E76.1
lipidosis
cerebral
E75.4
generalized
E75.6
mucopolysaccharidosis
Mucopolysaccharidosis
myxedema
E03.9
G32.89
neoplastic disease
D49.6
G32.89
Neoplasm
Niemann-Pick disease
E75.249
G32.89
sphingolipidosis
E75.3
G32.89
vitamin B12 deficiency
E53.8
G32.89
senile NEC
G31.1
breast
N64.89
Bruch's membrane
Degeneration, choroid
capillaries
(fatty)
I78.8
amyloid
E85.89
I79.8
cardiac
Degeneration, myocardial
valve, valvular
Endocarditis
cardiorenal
Hypertension, cardiorenal
cardiovascular
Disease, cardiovascular
renal
Hypertension, cardiorenal
cerebellar NOS
G31.9
alcoholic
G31.2
primary
(hereditary) (sporadic)
G11.9
cerebral
Degeneration, brain
cerebrovascular
I67.9
due to hypertension
I67.4
cervical plexus
G54.2
cervix
N88.8
due to radiation
(intended effect)
N88.8
adverse effect or misadventure
N99.89
chamber angle
H21.21-
changes, spine or vertebra
Spondylosis
chorioretinal
Degeneration, choroid
hereditary
H31.20
choroid
(colloid) (drusen)
H31.10-
atrophy
Atrophy, choroidal
hereditary
Dystrophy, choroidal, hereditary
ciliary body
H21.22-
cochlear
H83.8
combined
(spinal cord) (subacute)
E53.8
G32.0
with anemia
(pernicious)
D51.0
G32.0
due to dietary vitamin B12 deficiency
D51.3
G32.0
in
(due to)
vitamin B12 deficiency
E53.8
G32.0
anemia
D51.9
G32.0
conjunctiva
H11.10
concretions
Concretion, conjunctiva
deposits
Deposit, conjunctiva
pigmentations
Pigmentation, conjunctiva
pinguecula
Pinguecula
xerosis
Xerosis, conjunctiva
cornea
H18.40
calcerous
H18.43
band keratopathy
H18.42-
familial, hereditary
Dystrophy, cornea
hyaline
(of old scars)
H18.49
keratomalacia
Keratomalacia
nodular
H18.45-
peripheral
H18.46-
senile
H18.41-
specified type NEC
H18.49
cortical
(cerebellar) (parenchymatous)
G31.89
alcoholic
G31.2
diffuse, due to arteriopathy
I67.2
corticobasal
G31.85
cutis
L98.8
amyloid
E85.4
L99
dental pulp
K04.2
disc disease
Degeneration, intervertebral disc NEC
dorsolateral
(spinal cord)
Degeneration, combined
extrapyramidal
G25.9
eye, macular
Degeneration, macula
congenital or hereditary
Dystrophy, retina
facet joints
Spondylosis
fatty
liver NEC
K76.0
alcoholic
K70.0
grey matter
(brain) (Alpers')
G31.81
heart
Degeneration, myocardial
amyloid
E85.4
I43
atheromatous
Disease, heart, ischemic, atherosclerotic
ischemic
Disease, heart, ischemic
hepatolenticular
(Wilson's)
E83.01
hepatorenal
K76.7
hyaline
(diffuse) (generalized)
localized
Degeneration, by site
infrapatellar fat pad
M79.4
intervertebral disc NOS
with
myelopathy
Disorder, disc, with, myelopathy
radiculitis or radiculopathy
Disorder, disc, with, radiculopathy
cervical, cervicothoracic
Disorder, disc, cervical, degeneration
with
myelopathy
Disorder, disc, cervical, with myelopathy
neuritis, radiculitis or radiculopathy
Disorder, disc, cervical, with neuritis
lumbar region
M51.36
with
myelopathy
M51.06
neuritis, radiculitis, radiculopathy or sciatica
M51.16
lumbosacral region
M51.37
with
neuritis, radiculitis, radiculopathy or sciatica
M51.17
sacrococcygeal region
M53.3
thoracic region
M51.34
with
myelopathy
M51.04
neuritis, radiculitis, radiculopathy
M51.14
thoracolumbar region
M51.35
with
myelopathy
M51.05
neuritis, radiculitis, radiculopathy
M51.15
intestine, amyloid
E85.4
iris
(pigmentary)
H21.23-
ischemic
Ischemia
joint disease
Osteoarthritis
kidney
N28.89
amyloid
E85.4
N29
cystic, congenital
Q61.9
fatty
N28.89
polycystic
Q61.3
adult type
(autosomal dominant)
Q61.2
infantile type NEC
(autosomal recessive)
Q61.19
collecting duct dilatation
Q61.11
Kuhnt-Junius
H35.32-
Degeneration, macula
lens
Cataract
lenticular
(familial) (progressive) (Wilson's) (with cirrhosis of liver)
E83.01
liver NEC
(diffuse)
K76.89
amyloid
E85.4
K77
cystic
K76.89
congenital
Q44.6
fatty NEC
K76.0
alcoholic
K70.0
hypertrophic
K76.89
parenchymatous, acute or subacute
K72.00
with coma
K72.01
pigmentary
K76.89
toxic
(acute)
K71.9
lung
J98.4
lymph gland
I89.8
hyaline
I89.8
macula, macular
(acquired) (age-related) (senile)
H35.30
angioid streaks
H35.33
atrophic age-related
H35.31-
congenital or hereditary
Dystrophy, retina
cystoid
H35.35-
drusen
H35.36-
dry age-related
H35.31-
exudative
H35.32-
hole
H35.34-
nonexudative
H35.31-
puckering
H35.37-
toxic
H35.38-
wet age-related
H35.32-
membranous labyrinth, congenital
(causing impairment of hearing)
Q16.5
meniscus
Derangement, meniscus
mitral
Insufficiency, mitral
Mönckeberg's
Arteriosclerosis, extremities
motor centers, senile
G31.1
multi-system
G90.3
mural
Degeneration, myocardial
muscle
(fatty) (fibrous) (hyaline) (progressive)
M62.89
heart
Degeneration, myocardial
myelin, central nervous system
G37.9
myocardial, myocardium
(fatty) (hyaline) (senile)
I51.5
with rheumatic fever
(conditions in I00)
I09.0
active, acute or subacute
I01.2
with chorea
I02.0
inactive or quiescent
(with chorea)
I09.0
hypertensive
Hypertension, heart
rheumatic
Degeneration, myocardial, with rheumatic fever
syphilitic
A52.06
nasal sinus
(mucosa)
J32.9
frontal
J32.1
maxillary
J32.0
nerve
Disorder, nerve
nervous system
G31.9
alcoholic
G31.2
amyloid
E85.4
G99.8
autonomic
G90.9
fatty
G31.89
specified NEC
G31.89
nipple
N64.89
olivopontocerebellar
(hereditary) (familial)
G23.8
osseous labyrinth
H83.8
ovary
N83.8
cystic
N83.20-
microcystic
N83.20-
pallidal pigmentary
(progressive)
G23.0
pancreas
K86.89
tuberculous
A18.83
penis
N48.89
pigmentary
(diffuse) (general)
localized
Degeneration, by site
pallidal
(progressive)
G23.0
pineal gland
E34.8
pituitary
(gland)
E23.6
popliteal fat pad
M79.4
posterolateral
(spinal cord)
Degeneration, combined
pulmonary valve
(heart)
I37.8
pulp
(tooth)
K04.2
pupillary margin
H21.24-
renal
Degeneration, kidney
retina
H35.9
hereditary
(cerebroretinal) (congenital) (juvenile) (macula) (peripheral) (pigmentary)
Dystrophy, retina
Kuhnt-Junius
H35.32-
Degeneration, macula
macula
(cystic) (exudative) (hole) (nonexudative) (pseudohole) (senile) (toxic)
Degeneration, macula
peripheral
H35.40
lattice
H35.41-
microcystoid
H35.42-
paving stone
H35.43-
secondary
pigmentary
H35.45-
vitreoretinal
H35.46-
senile reticular
H35.44-
pigmentary
(primary)
Dystrophy, retina
secondary
Degeneration, retina, peripheral, secondary
posterior pole
Degeneration, macula
saccule, congenital
(causing impairment of hearing)
Q16.5
senile
R54
brain
G31.1
cardiac, heart or myocardium
Degeneration, myocardial
motor centers
G31.1
vascular
Arteriosclerosis
sinus
(cystic)
Sinusitis
polypoid
J33.1
skin
L98.8
amyloid
E85.4
L99
colloid
L98.8
spinal
(cord)
G31.89
amyloid
E85.4
G32.89
combined
(subacute)
Degeneration, combined
dorsolateral
Degeneration, combined
familial NEC
G31.89
fatty
G31.89
funicular
Degeneration, combined
posterolateral
Degeneration, combined
subacute combined
Degeneration, combined
tuberculous
A17.81
spleen
D73.0
amyloid
E85.4
D77
stomach
K31.89
striatonigral
G23.2
suprarenal
(capsule) (gland)
E27.8
synovial membrane
(pulpy)
Disorder, synovium, specified type NEC
tapetoretinal
Dystrophy, retina
thymus
(gland)
E32.8
fatty
E32.8
thyroid
(gland)
E07.89
tricuspid
(heart) (valve)
I07.9
tuberculous NEC
Tuberculosis
turbinate
J34.89
uterus
(cystic)
N85.8
vascular
(senile)
Arteriosclerosis
hypertensive
Hypertension
vitreoretinal, secondary
Degeneration, retina, peripheral, secondary, vitreoretinal
vitreous
(body)
H43.81-
Wallerian
Disorder, nerve
Wilson's hepatolenticular
E83.01