Alphabetic Index · main term

Degeneration, degenerative

FY2027Index: De /Alphabetic Index

Degeneration, degenerative is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). It has 290 subterms and 198 code entries. First-level subterms include adrenal, amyloid, anterior cornua, spinal cord, anterior labral, aorta, aortic, aortic valve, arteriovascular, artery, arterial and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 290

adrenal (capsule) (fatty) (gland) (hyaline) (infectional)E27.8
amyloid see also AmyloidosisE85.9
anterior cornua, spinal cordG12.29
anterior labralS43.49-
aorta, aorticI70.0
- fattyI77.89
aortic valve (heart) see Endocarditis, aortic
arteriovascular see Arteriosclerosis
artery, arterial (atheromatous) (calcareous) see also Arteriosclerosis
- cerebral, amyloidE85.4[I68.0]
- medial see Arteriosclerosis, extremities
articular cartilage NEC see Derangement, joint, articular cartilage, by site
atheromatous see Arteriosclerosis
basal nuclei or gangliaG23.9
- specified NECG23.8
bone NEC see Disorder, bone, specified type NEC
brachial plexusG54.0
brain (cortical) (progressive)G31.9
- alcoholicG31.2
- arterioscleroticI67.2
- childhoodG31.9
  - specified NECG31.89
- cysticG31.89
  - congenitalQ04.6
- in
  - alcoholismG31.2
  - beriberiE51.2
  - cerebrovascular diseaseI67.9
  - congenital hydrocephalusQ03.9
    with spina bifida see also Spina bifida
  - Fabry-Anderson diseaseE75.21
  - Gaucher's diseaseE75.22
  - Hunter's syndromeE76.1
  - lipidosis
    cerebralE75.4
    generalizedE75.6
  - mucopolysaccharidosis see Mucopolysaccharidosis
  - myxedemaE03.9[G32.89]
  - neoplastic disease see also NeoplasmD49.6[G32.89]
  - Niemann-Pick diseaseE75.249[G32.89]
  - sphingolipidosisE75.3[G32.89]
  - vitamin B12 deficiencyE53.8[G32.89]
- senile NECG31.1
breastN64.89
Bruch's membrane see Degeneration, choroid
capillaries (fatty)I78.8
- amyloidE85.89[I79.8]
cardiac see also Degeneration, myocardial
- valve, valvular see Endocarditis
cardiorenal see Hypertension, cardiorenal
cardiovascular see also Disease, cardiovascular
- renal see Hypertension, cardiorenal
cerebellar NOSG31.9
- alcoholicG31.2
- primary (hereditary) (sporadic)G11.9
cerebral see Degeneration, brain
cerebrovascularI67.9
- due to hypertensionI67.4
cervical plexusG54.2
cervixN88.8
- due to radiation (intended effect)N88.8
  - adverse effect or misadventureN99.89
chamber angleH21.21-
changes, spine or vertebra see Spondylosis
chorioretinal see also Degeneration, choroid
- hereditaryH31.20
choroid (colloid) (drusen)H31.10-
- atrophy see Atrophy, choroidal
- hereditary see Dystrophy, choroidal, hereditary
ciliary bodyH21.22-
cochlearH83.8-
combined (spinal cord) (subacute)E53.8[G32.0]
- with anemia (pernicious)D51.0[G32.0]
  - due to dietary vitamin B12 deficiencyD51.3[G32.0]
- in (due to)
  - vitamin B12 deficiencyE53.8[G32.0]
    anemiaD51.9[G32.0]
conjunctivaH11.10
- concretions see Concretion, conjunctiva
- deposits see Deposit, conjunctiva
- pigmentations see Pigmentation, conjunctiva
- pinguecula see Pinguecula
- xerosis see Xerosis, conjunctiva
corneaH18.40
- calcerousH18.43
  - band keratopathyH18.42-
- familial, hereditary see Dystrophy, cornea
- hyaline (of old scars)H18.49
- keratomalacia see Keratomalacia
- nodularH18.45-
- peripheralH18.46-
- senileH18.41-
- specified type NECH18.49
cortical (cerebellar) (parenchymatous)G31.89
- alcoholicG31.2
- diffuse, due to arteriopathyI67.2
corticobasalG31.85
cutisL98.8
- amyloidE85.4[L99]
dental pulpK04.2
disc disease see Degeneration, intervertebral disc, by site
dorsolateral (spinal cord) see Degeneration, combined
extrapyramidalG25.9
eye, macular see also Degeneration, macula
- congenital or hereditary see Dystrophy, retina
facet joints see Spondylosis
fatty
- liver NECK76.0
  - alcoholicK70.0
grey matter (brain) (Alpers')G31.81
heart see also Degeneration, myocardial
- amyloidE85.4[I43]
- atheromatous see Disease, heart, ischemic, atherosclerotic
- ischemic see Disease, heart, ischemic
hepatolenticular (Wilson's)E83.01
hepatorenalK76.7
hyaline (diffuse) (generalized)
- localized see Degeneration, by site
infrapatellar fat padM79.4
intervertebral disc
- with
  - myelopathy see Disorder, disc, with, myelopathy
  - radiculitis or radiculopathy see Disorder, disc, with, radiculopathy
- cervical, cervicothoracic see Disorder, disc, cervical, degeneration
  - with
    myelopathy see Disorder, disc, cervical, with myelopathy
    neuritis, radiculitis or radiculopathy see Disorder, disc, cervical, with neuritis
- lumbar regionM51.36-
  - with
    myelopathyM51.06
    neuritis, radiculitis, radiculopathy or sciaticaM51.16
- lumbosacral regionM51.37-
  - with
    neuritis, radiculitis, radiculopathy or sciaticaM51.17
- sacrococcygeal regionM53.3
- thoracic regionM51.34
  - with
    myelopathyM51.04
    neuritis, radiculitis, radiculopathyM51.14
- thoracolumbar regionM51.35
  - with
    myelopathyM51.05
    neuritis, radiculitis, radiculopathyM51.15
intestine, amyloidE85.4
iris (pigmentary)H21.23-
ischemic see Ischemia
joint disease see Osteoarthritis
kidneyN28.89
- amyloidE85.4[N29]
- cystic, congenitalQ61.9
- fattyN28.89
- polycysticQ61.3
  - adult type (autosomal dominant)Q61.2
  - infantile type (autosomal recessive) NECQ61.19
    collecting duct dilatationQ61.11
Kuhnt-Junius see also Degeneration, maculaH35.32-
lens see Cataract
lenticular (familial) (progressive) (Wilson's) (with cirrhosis of liver)E83.01
liver (diffuse) NECK76.89
- amyloidE85.4[K77]
- cysticK76.89
  - congenitalQ44.6
- fatty NECK76.0
  - alcoholicK70.0
- hypertrophicK76.89
- parenchymatous, acute or subacuteK72.00
  - with comaK72.01
- pigmentaryK76.89
- toxic (acute)K71.9
lungJ98.4
lymph glandI89.8
- hyalineI89.8
macula, macular (acquired) (age-related) (senile)H35.30
- angioid streaksH35.33
- atrophic age-relatedH35.31-
- congenital or hereditary see Dystrophy, retina
- cystoidH35.35-
- drusenH35.36-
- dry age-relatedH35.31-
- exudativeH35.32-
- holeH35.34-
- nonexudativeH35.31-
- puckeringH35.37-
- toxicH35.38-
- wet age-relatedH35.32-
membranous labyrinth, congenital (causing impairment of hearing)Q16.5
meniscus see Derangement, meniscus
mitral see Insufficiency, mitral
Mönckeberg's see Arteriosclerosis, extremities
motor centers, senileG31.1
multi-systemG90.3
mural see Degeneration, myocardial
muscle (fatty) (fibrous) (hyaline) (progressive)M62.89
- heart see Degeneration, myocardial
myelin, central nervous systemG37.9
myocardial, myocardium (fatty) (hyaline) (senile)I51.5
- with rheumatic fever (conditions in I00)I09.0
  - active, acute or subacuteI01.2
    with choreaI02.0
  - inactive or quiescent (with chorea)I09.0
- hypertensive see Hypertension, heart
- rheumatic see Degeneration, myocardial, with rheumatic fever
- syphiliticA52.06
nasal sinus (mucosa)J32.9
- frontalJ32.1
- maxillaryJ32.0
nerve see Disorder, nerve
nervous systemG31.9
- alcoholicG31.2
- amyloidE85.4[G99.8]
- autonomicG90.9
- fattyG31.89
- specified NECG31.89
nippleN64.89
olivopontocerebellar (hereditary) (familial)G23.8
osseous labyrinthH83.8-
ovaryN83.8
- cysticN83.20-
- microcysticN83.20-
pallidal pigmentary (progressive)G23.0
pancreasK86.89
- tuberculousA18.83
penisN48.89
pigmentary (diffuse) (general)
- localized see Degeneration, by site
- pallidal (progressive)G23.0
pineal glandE34.8
pituitary (gland)E23.6
popliteal fat padM79.4
posterolateral (spinal cord) see Degeneration, combined
pulmonary valve (heart)I37.8
pulp (tooth)K04.2
pupillary marginH21.24-
renal see Degeneration, kidney
retinaH35.9
- hereditary (cerebroretinal) (congenital) (juvenile) (macula) (peripheral) (pigmentary) see Dystrophy, retina
- Kuhnt-Junius see also Degeneration, maculaH35.32-
- macula (cystic) (exudative) (hole) (nonexudative) (pseudohole) (senile) (toxic) see Degeneration, macula
- peripheralH35.40
  - latticeH35.41-
  - microcystoidH35.42-
  - paving stoneH35.43-
  - secondary
    pigmentaryH35.45-
    vitreoretinalH35.46-
  - senile reticularH35.44-
- pigmentary (primary) see also Dystrophy, retina
  - secondary see Degeneration, retina, peripheral, secondary
- posterior pole see Degeneration, macula
saccule, congenital (causing impairment of hearing)Q16.5
senileR54
- brainG31.1
- cardiac, heart or myocardium see Degeneration, myocardial
- motor centersG31.1
- vascular see Arteriosclerosis
sinus (cystic) see also Sinusitis
- polypoidJ33.1
skinL98.8
- amyloidE85.4[L99]
- colloidL98.8
spinal (cord)G31.89
- amyloidE85.4[G32.89]
- combined (subacute) see Degeneration, combined
- dorsolateral see Degeneration, combined
- familial NECG31.89
- fattyG31.89
- funicular see Degeneration, combined
- posterolateral see Degeneration, combined
- subacute combined see Degeneration, combined
- tuberculousA17.81
spleenD73.0
- amyloidE85.4[D77]
stomachK31.89
striatonigralG23.2
suprarenal (capsule) (gland)E27.8
synovial membrane (pulpy) see Disorder, synovium, specified type NEC
tapetoretinal see Dystrophy, retina
thymus (gland)E32.8
- fattyE32.8
thyroid (gland)E07.89
tricuspid (heart) (valve)I07.9
tuberculous NEC see Tuberculosis
turbinateJ34.89
uterus (cystic)N85.8
vascular (senile) see Arteriosclerosis
- hypertensive see Hypertension
vitreoretinal, secondary see Degeneration, retina, peripheral, secondary, vitreoretinal
vitreous (body)H43.81-
Wallerian see Disorder, nerve
Wilson's hepatolenticularE83.01