ICD-10-CM Alphabetic Index to Diseases and Injuries
Degeneration, degenerative
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- adrenal (capsule) (fatty) (gland) (hyaline) (infectional) E27.8
- amyloid E85.9 — see also Amyloidosis
- anterior cornua, spinal cord G12.29
- anterior labral S43.49-
- aorta, aortic I70.0
- fatty I77.89
- aortic valve (heart) — see Endocarditis, aortic
- arteriovascular — see Arteriosclerosis
- artery, arterial (atheromatous) (calcareous) — see also Arteriosclerosis
- cerebral, amyloid E85.4
- medial — see Arteriosclerosis, extremities
- articular cartilage NEC — see Derangement, joint, articular cartilage, by site
- atheromatous — see Arteriosclerosis
- basal nuclei or ganglia G23.9
- specified NEC G23.8
- bone NEC — see 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 — see also 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 — see Mucopolysaccharidosis
- myxedema E03.9
- neoplastic disease D49.6 — see also Neoplasm
- Niemann-Pick disease E75.249
- sphingolipidosis E75.3
- vitamin B12 deficiency E53.8
- senile NEC G31.1
- breast N64.89
- Bruch's membrane — see Degeneration, choroid
- capillaries (fatty) I78.8
- amyloid E85.89
- cardiac — see also Degeneration, myocardial
- valve, valvular — see Endocarditis
- cardiorenal — see Hypertension, cardiorenal
- cardiovascular — see also Disease, cardiovascular
- renal — see Hypertension, cardiorenal
- cerebellar NOS G31.9
- alcoholic G31.2
- primary (hereditary) (sporadic) G11.9
- cerebral — see 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 — see Spondylosis
- chorioretinal — see also Degeneration, choroid
- hereditary H31.20
- choroid (colloid) (drusen) H31.10-
- atrophy — see Atrophy, choroidal
- hereditary — see Dystrophy, choroidal, hereditary
- ciliary body H21.22-
- cochlear
- combined (spinal cord) (subacute) E53.8
- with anemia (pernicious) D51.0
- due to dietary vitamin B12 deficiency D51.3
- in (due to)
- vitamin B12 deficiency E53.8
- anemia D51.9
- conjunctiva H11.10
- concretions — see Concretion, conjunctiva
- deposits — see Deposit, conjunctiva
- pigmentations — see Pigmentation, conjunctiva
- pinguecula — see Pinguecula
- xerosis — see Xerosis, conjunctiva
- cornea H18.40
- calcerous H18.43
- band keratopathy H18.42-
- familial, hereditary — see Dystrophy, cornea
- hyaline (of old scars) H18.49
- keratomalacia — see 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
- dental pulp K04.2
- disc disease — see Degeneration, intervertebral disc, by site
- dorsolateral (spinal cord) — see Degeneration, combined
- extrapyramidal G25.9
- eye, macular — see also Degeneration, macula
- congenital or hereditary — see Dystrophy, retina
- facet joints — see Spondylosis
- fatty
- liver NEC K76.0
- alcoholic K70.0
- grey matter (brain) (Alpers') G31.81
- heart — see also Degeneration, myocardial
- amyloid E85.4
- atheromatous — see Disease, heart, ischemic, atherosclerotic
- ischemic — see Disease, heart, ischemic
- hepatolenticular (Wilson's) E83.01
- hepatorenal K76.7
- hyaline (diffuse) (generalized)
- localized — see Degeneration, by site
- infrapatellar fat pad M79.4
- 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 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 — see Ischemia
- joint disease — see Osteoarthritis
- kidney N28.89
- amyloid E85.4
- cystic, congenital Q61.9
- fatty N28.89
- polycystic Q61.3
- adult type (autosomal dominant) Q61.2
- infantile type (autosomal recessive) NEC Q61.19
- collecting duct dilatation Q61.11
- Kuhnt-Junius H35.32- — see also Degeneration, macula
- lens — see Cataract
- lenticular (familial) (progressive) (Wilson's) (with cirrhosis of liver) E83.01
- liver (diffuse) NEC K76.89
- amyloid E85.4
- 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 — see 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 — see Derangement, meniscus
- mitral — see Insufficiency, mitral
- Mönckeberg's — see Arteriosclerosis, extremities
- motor centers, senile G31.1
- multi-system G90.3
- mural — see Degeneration, myocardial
- muscle (fatty) (fibrous) (hyaline) (progressive) M62.89
- heart — see 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 — see Hypertension, heart
- rheumatic — see Degeneration, myocardial, with rheumatic fever
- syphilitic A52.06
- nasal sinus (mucosa) J32.9
- frontal J32.1
- maxillary J32.0
- nerve — see Disorder, nerve
- nervous system G31.9
- alcoholic G31.2
- amyloid E85.4
- autonomic G90.9
- fatty G31.89
- specified NEC G31.89
- nipple N64.89
- olivopontocerebellar (hereditary) (familial) G23.8
- osseous labyrinth
- 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 — see Degeneration, by site
- pallidal (progressive) G23.0
- pineal gland E34.8
- pituitary (gland) E23.6
- popliteal fat pad M79.4
- posterolateral (spinal cord) — see Degeneration, combined
- pulmonary valve (heart) I37.8
- pulp (tooth) K04.2
- pupillary margin H21.24-
- renal — see Degeneration, kidney
- retina H35.9
- hereditary (cerebroretinal) (congenital) (juvenile) (macula) (peripheral) (pigmentary) — see Dystrophy, retina
- Kuhnt-Junius H35.32- — see also Degeneration, macula
- macula (cystic) (exudative) (hole) (nonexudative) (pseudohole) (senile) (toxic) — see 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) — see also Dystrophy, retina
- secondary — see Degeneration, retina, peripheral, secondary
- posterior pole — see Degeneration, macula
- saccule, congenital (causing impairment of hearing) Q16.5
- senile R54
- brain G31.1
- cardiac, heart or myocardium — see Degeneration, myocardial
- motor centers G31.1
- vascular — see Arteriosclerosis
- sinus (cystic) — see also Sinusitis
- polypoid J33.1
- skin L98.8
- amyloid E85.4
- colloid L98.8
- spinal (cord) G31.89
- amyloid E85.4
- combined (subacute) — see Degeneration, combined
- dorsolateral — see Degeneration, combined
- familial NEC G31.89
- fatty G31.89
- funicular — see Degeneration, combined
- posterolateral — see Degeneration, combined
- subacute combined — see Degeneration, combined
- tuberculous A17.81
- spleen D73.0
- amyloid E85.4
- stomach K31.89
- striatonigral G23.2
- suprarenal (capsule) (gland) E27.8
- synovial membrane (pulpy) — see Disorder, synovium, specified type NEC
- tapetoretinal — see Dystrophy, retina
- thymus (gland) E32.8
- fatty E32.8
- thyroid (gland) E07.89
- tricuspid (heart) (valve) I07.9
- tuberculous NEC — see Tuberculosis
- turbinate J34.89
- 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 hepatolenticular E83.01