Degeneration, degenerative

"Degeneration, degenerative" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "degeneration, degenerative"

  • Degeneration, degenerative
    • adrenal (capsule) (fatty) (gland) (hyaline) (infectional) - E27.8 Other specified disorders of adrenal gland
    • amyloid - See Also: Amyloidosis; - E85.9 Amyloidosis, unspecified
    • anterior cornua, spinal cord - G12.29 Other motor neuron disease
    • anterior labral - S43.49 Other sprain of shoulder joint
    • aorta, aortic - I70.0 Atherosclerosis of aorta
      • fatty - I77.89 Other specified disorders of arteries and arterioles
    • aortic valve (heart) - See: Endocarditis, aortic;
    • arteriovascular - See: Arteriosclerosis;
    • artery, arterial (atheromatous) (calcareous) - See Also: Arteriosclerosis;
      • cerebral, amyloid - E85.4 Organ-limited amyloidosis
      • medial - See: Arteriosclerosis, extremities;
    • articular cartilage NEC - See: Derangement, joint, articular cartilage, by site;
    • atheromatous - See: Arteriosclerosis;
    • basal nuclei or ganglia - G23.9 Degenerative disease of basal ganglia, unspecified
      • specified NEC - G23.8 Other specified degenerative diseases of basal ganglia
    • bone NEC - See: Disorder, bone, specified type NEC;
    • brachial plexus - G54.0 Brachial plexus disorders
    • brain (cortical) (progressive) - G31.9 Degenerative disease of nervous system, unspecified
      • alcoholic - G31.2 Degeneration of nervous system due to alcohol
      • arteriosclerotic - I67.2 Cerebral atherosclerosis
      • childhood - G31.9 Degenerative disease of nervous system, unspecified
        • specified NEC - G31.89 Other specified degenerative diseases of nervous system
      • cystic - G31.89 Other specified degenerative diseases of nervous system
        • congenital - Q04.6 Congenital cerebral cysts
      • in
        • alcoholism - G31.2 Degeneration of nervous system due to alcohol
        • beriberi - E51.2 Wernicke's encephalopathy
        • cerebrovascular disease - I67.9 Cerebrovascular disease, unspecified
        • congenital hydrocephalus - Q03.9 Congenital hydrocephalus, unspecified
          • with spina bifida - See Also: Spina bifida;
        • Fabry-Anderson disease - E75.21 Fabry (-Anderson) disease
        • Gaucher's disease - E75.22 Gaucher disease
        • Hunter's syndrome - E76.1 Mucopolysaccharidosis, type II
        • lipidosis
          • cerebral - E75.4 Neuronal ceroid lipofuscinosis
          • generalized - E75.6 Lipid storage disorder, unspecified
        • mucopolysaccharidosis - See: Mucopolysaccharidosis;
        • myxedema - E03.9 Hypothyroidism, unspecified
        • neoplastic disease - See Also: Neoplasm; - D49.6 Neoplasm of unspecified behavior of brain
        • Niemann-Pick disease - E75.249 Niemann-Pick disease, unspecified
        • sphingolipidosis - E75.3 Sphingolipidosis, unspecified
        • vitamin B12 deficiency - E53.8 Deficiency of other specified B group vitamins
      • senile NEC - G31.1 Senile degeneration of brain, not elsewhere classified
    • breast - N64.89 Other specified disorders of breast
    • Bruch's membrane - See: Degeneration, choroid;
    • capillaries (fatty) - I78.8 Other diseases of capillaries
      • amyloid - E85.89 Other amyloidosis
    • 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 Degenerative disease of nervous system, unspecified
      • alcoholic - G31.2 Degeneration of nervous system due to alcohol
      • primary (hereditary) (sporadic) - G11.9 Hereditary ataxia, unspecified
    • cerebral - See: Degeneration, brain;
    • cerebrovascular - I67.9 Cerebrovascular disease, unspecified
      • due to hypertension - I67.4 Hypertensive encephalopathy
    • cervical plexus - G54.2 Cervical root disorders, not elsewhere classified
    • cervix - N88.8 Other specified noninflammatory disorders of cervix uteri
      • due to radiation (intended effect) - N88.8 Other specified noninflammatory disorders of cervix uteri
        • adverse effect or misadventure - N99.89 Other postprocedural complications and disorders of genitourinary system
    • chamber angle - H21.21 Degeneration of chamber angle
    • changes, spine or vertebra - See: Spondylosis;
    • chorioretinal - See Also: Degeneration, choroid;
      • hereditary - H31.20 Hereditary choroidal dystrophy, unspecified
    • choroid (colloid) (drusen) - H31.10 Unspecified choroidal degeneration
      • atrophy - See: Atrophy, choroidal;
      • hereditary - See: Dystrophy, choroidal, hereditary;
    • ciliary body - H21.22 Degeneration of ciliary body
    • cochlear
    • combined (spinal cord) (subacute) - E53.8 Deficiency of other specified B group vitamins
      • in (due to)
        • vitamin B12 deficiency - E53.8 Deficiency of other specified B group vitamins
          • anemia - D51.9 Vitamin B12 deficiency anemia, unspecified
      • with anemia (pernicious) - D51.0 Vitamin B12 deficiency anemia due to intrinsic factor deficiency
        • due to dietary vitamin B12 deficiency - D51.3 Other dietary vitamin B12 deficiency anemia
    • conjunctiva - H11.10 Unspecified conjunctival degenerations
      • concretions - See: Concretion, conjunctiva;
      • deposits - See: Deposit, conjunctiva;
      • pigmentations - See: Pigmentation, conjunctiva;
      • pinguecula - See: Pinguecula;
      • xerosis - See: Xerosis, conjunctiva;
    • cornea - H18.40 Unspecified corneal degeneration
      • calcerous - H18.43 Other calcerous corneal degeneration
        • band keratopathy - H18.42 Band keratopathy
      • familial, hereditary - See: Dystrophy, cornea;
      • hyaline (of old scars) - H18.49 Other corneal degeneration
      • keratomalacia - See: Keratomalacia;
      • nodular - H18.45 Nodular corneal degeneration
      • peripheral - H18.46 Peripheral corneal degeneration
      • senile - H18.41 Arcus senilis
      • specified type NEC - H18.49 Other corneal degeneration
    • cortical (cerebellar) (parenchymatous) - G31.89 Other specified degenerative diseases of nervous system
      • alcoholic - G31.2 Degeneration of nervous system due to alcohol
      • diffuse, due to arteriopathy - I67.2 Cerebral atherosclerosis
    • corticobasal - G31.85 Corticobasal degeneration
    • cutis - L98.8 Other specified disorders of the skin and subcutaneous tissue
      • amyloid - E85.4 Organ-limited amyloidosis
    • dental pulp - K04.2 Pulp degeneration
    • disc disease - See: Degeneration, intervertebral disc, by site;
    • dorsolateral (spinal cord) - See: Degeneration, combined;
    • extrapyramidal - G25.9 Extrapyramidal and movement disorder, unspecified
    • eye, macular - See Also: Degeneration, macula;
      • congenital or hereditary - See: Dystrophy, retina;
    • facet joints - See: Spondylosis;
    • fatty
      • liver NEC - K76.0 Fatty (change of) liver, not elsewhere classified
        • alcoholic - K70.0 Alcoholic fatty liver
    • grey matter (brain) (Alpers') - G31.81 Alpers disease
    • heart - See Also: Degeneration, myocardial;
      • amyloid - E85.4 Organ-limited amyloidosis
      • atheromatous - See: Disease, heart, ischemic, atherosclerotic;
      • ischemic - See: Disease, heart, ischemic;
    • hepatolenticular (Wilson's) - E83.01 Wilson's disease
    • hepatorenal - K76.7 Hepatorenal syndrome
    • hyaline (diffuse) (generalized)
      • localized - See: Degeneration, by site;
    • infrapatellar fat pad - M79.4 Hypertrophy of (infrapatellar) fat pad
    • intervertebral disc NOS
      • 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 Other intervertebral disc degeneration, lumbar region
        • with
          • myelopathy - M51.06 Intervertebral disc disorders with myelopathy, lumbar region
          • neuritis, radiculitis, radiculopathy or sciatica - M51.16 Intervertebral disc disorders with radiculopathy, lumbar region
      • lumbosacral region - M51.37 Other intervertebral disc degeneration, lumbosacral region
        • with
          • neuritis, radiculitis, radiculopathy or sciatica - M51.17 Intervertebral disc disorders with radiculopathy, lumbosacral region
      • sacrococcygeal region - M53.3 Sacrococcygeal disorders, not elsewhere classified
      • thoracic region - M51.34 Other intervertebral disc degeneration, thoracic region
        • with
          • myelopathy - M51.04 Intervertebral disc disorders with myelopathy, thoracic region
          • neuritis, radiculitis, radiculopathy - M51.14 Intervertebral disc disorders with radiculopathy, thoracic region
      • thoracolumbar region - M51.35 Other intervertebral disc degeneration, thoracolumbar region
        • with
          • myelopathy - M51.05 Intervertebral disc disorders with myelopathy, thoracolumbar region
          • neuritis, radiculitis, radiculopathy - M51.15 Intervertebral disc disorders with radiculopathy, thoracolumbar region
      • with
        • myelopathy - See: Disorder, disc, with, myelopathy;
        • radiculitis or radiculopathy - See: Disorder, disc, with, radiculopathy;
    • intestine, amyloid - E85.4 Organ-limited amyloidosis
    • iris (pigmentary) - H21.23 Degeneration of iris (pigmentary)
    • ischemic - See: Ischemia;
    • joint disease - See: Osteoarthritis;
    • kidney - N28.89 Other specified disorders of kidney and ureter
      • amyloid - E85.4 Organ-limited amyloidosis
      • cystic, congenital - Q61.9 Cystic kidney disease, unspecified
      • fatty - N28.89 Other specified disorders of kidney and ureter
      • polycystic - Q61.3 Polycystic kidney, unspecified
        • adult type (autosomal dominant) - Q61.2 Polycystic kidney, adult type
        • infantile type (autosomal recessive) NEC - Q61.19 Other polycystic kidney, infantile type
          • collecting duct dilatation - Q61.11 Cystic dilatation of collecting ducts
    • Kuhnt-Junius - See Also: Degeneration, macula; - H35.32 Exudative age-related macular degeneration
    • lens - See: Cataract;
    • lenticular (familial) (progressive) (Wilson's) (with cirrhosis of liver) - E83.01 Wilson's disease
    • liver (diffuse) NEC - K76.89 Other specified diseases of liver
      • amyloid - E85.4 Organ-limited amyloidosis
      • cystic - K76.89 Other specified diseases of liver
        • congenital - Q44.6 Cystic disease of liver
      • fatty NEC - K76.0 Fatty (change of) liver, not elsewhere classified
        • alcoholic - K70.0 Alcoholic fatty liver
      • hypertrophic - K76.89 Other specified diseases of liver
      • parenchymatous, acute or subacute - K72.00 Acute and subacute hepatic failure without coma
        • with coma - K72.01 Acute and subacute hepatic failure with coma
      • pigmentary - K76.89 Other specified diseases of liver
      • toxic (acute) - K71.9 Toxic liver disease, unspecified
    • lung - J98.4 Other disorders of lung
    • lymph gland - I89.8 Other specified noninfective disorders of lymphatic vessels and lymph nodes
      • hyaline - I89.8 Other specified noninfective disorders of lymphatic vessels and lymph nodes
    • membranous labyrinth, congenital (causing impairment of hearing) - Q16.5 Congenital malformation of inner ear
    • meniscus - See: Derangement, meniscus;
    • mitral - See: Insufficiency, mitral;
    • Mönckeberg's - See: Arteriosclerosis, extremities;
    • motor centers, senile - G31.1 Senile degeneration of brain, not elsewhere classified
    • multi-system - G90.3 Multi-system degeneration of the autonomic nervous system
    • mural - See: Degeneration, myocardial;
    • muscle (fatty) (fibrous) (hyaline) (progressive) - M62.89 Other specified disorders of muscle
      • heart - See: Degeneration, myocardial;
    • myelin, central nervous system - G37.9 Demyelinating disease of central nervous system, unspecified
    • myocardial, myocardium (fatty) (hyaline) (senile) - I51.5 Myocardial degeneration
      • hypertensive - See: Hypertension, heart;
      • rheumatic - See: Degeneration, myocardial, with rheumatic fever;
      • syphilitic - A52.06 Other syphilitic heart involvement
      • with rheumatic fever (conditions in I00) - I09.0 Rheumatic myocarditis
        • active, acute or subacute - I01.2 Acute rheumatic myocarditis
          • with chorea - I02.0 Rheumatic chorea with heart involvement
        • inactive or quiescent (with chorea) - I09.0 Rheumatic myocarditis
    • nasal sinus (mucosa) - J32.9 Chronic sinusitis, unspecified
      • frontal - J32.1 Chronic frontal sinusitis
      • maxillary - J32.0 Chronic maxillary sinusitis
    • nerve - See: Disorder, nerve;
    • nervous system - G31.9 Degenerative disease of nervous system, unspecified
      • alcoholic - G31.2 Degeneration of nervous system due to alcohol
      • amyloid - E85.4 Organ-limited amyloidosis
      • autonomic - G90.9 Disorder of the autonomic nervous system, unspecified
      • fatty - G31.89 Other specified degenerative diseases of nervous system
      • specified NEC - G31.89 Other specified degenerative diseases of nervous system
    • nipple - N64.89 Other specified disorders of breast
    • olivopontocerebellar (hereditary) (familial) - G23.8 Other specified degenerative diseases of basal ganglia
    • osseous labyrinth
    • ovary - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
      • cystic - N83.20 Unspecified ovarian cysts
      • microcystic - N83.20 Unspecified ovarian cysts
    • pallidal pigmentary (progressive) - G23.0 Hallervorden-Spatz disease
    • pancreas - K86.89 Other specified diseases of pancreas
      • tuberculous - A18.83 Tuberculosis of digestive tract organs, not elsewhere classified
    • penis - N48.89 Other specified disorders of penis
    • pigmentary (diffuse) (general)
      • localized - See: Degeneration, by site;
      • pallidal (progressive) - G23.0 Hallervorden-Spatz disease
    • pineal gland - E34.8 Other specified endocrine disorders
    • pituitary (gland) - E23.6 Other disorders of pituitary gland
    • popliteal fat pad - M79.4 Hypertrophy of (infrapatellar) fat pad
    • posterolateral (spinal cord) - See: Degeneration, combined;
    • pulmonary valve (heart) - I37.8 Other nonrheumatic pulmonary valve disorders
    • pulp (tooth) - K04.2 Pulp degeneration
    • pupillary margin - H21.24 Degeneration of pupillary margin
    • renal - See: Degeneration, kidney;
    • retina - H35.9 Unspecified retinal disorder
      • hereditary (cerebroretinal) (congenital) (juvenile) (macula) (peripheral) (pigmentary) - See: Dystrophy, retina;
      • Kuhnt-Junius - See Also: Degeneration, macula; - H35.32 Exudative age-related macular degeneration
      • macula (cystic) (exudative) (hole) (nonexudative) (pseudohole) (senile) (toxic) - See: Degeneration, macula;
      • peripheral - H35.40 Unspecified peripheral retinal degeneration
        • lattice - H35.41 Lattice degeneration of retina
        • microcystoid - H35.42 Microcystoid degeneration of retina
        • paving stone - H35.43 Paving stone degeneration of retina
        • secondary
          • pigmentary - H35.45 Secondary pigmentary degeneration
          • vitreoretinal - H35.46 Secondary vitreoretinal degeneration
        • senile reticular - H35.44 Age-related reticular degeneration of retina
      • 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 Congenital malformation of inner ear
    • senile - R54 Age-related physical debility
      • brain - G31.1 Senile degeneration of brain, not elsewhere classified
      • cardiac, heart or myocardium - See: Degeneration, myocardial;
      • motor centers - G31.1 Senile degeneration of brain, not elsewhere classified
      • vascular - See: Arteriosclerosis;
    • sinus (cystic) - See Also: Sinusitis;
      • polypoid - J33.1 Polypoid sinus degeneration
    • skin - L98.8 Other specified disorders of the skin and subcutaneous tissue
      • amyloid - E85.4 Organ-limited amyloidosis
      • colloid - L98.8 Other specified disorders of the skin and subcutaneous tissue
    • spinal (cord) - G31.89 Other specified degenerative diseases of nervous system
      • amyloid - E85.4 Organ-limited amyloidosis
      • combined (subacute) - See: Degeneration, combined;
      • dorsolateral - See: Degeneration, combined;
      • familial NEC - G31.89 Other specified degenerative diseases of nervous system
      • fatty - G31.89 Other specified degenerative diseases of nervous system
      • funicular - See: Degeneration, combined;
      • posterolateral - See: Degeneration, combined;
      • subacute combined - See: Degeneration, combined;
      • tuberculous - A17.81 Tuberculoma of brain and spinal cord
    • spleen - D73.0 Hyposplenism
      • amyloid - E85.4 Organ-limited amyloidosis
    • stomach - K31.89 Other diseases of stomach and duodenum
    • striatonigral - G23.2 Striatonigral degeneration
    • suprarenal (capsule) (gland) - E27.8 Other specified disorders of adrenal gland
    • synovial membrane (pulpy) - See: Disorder, synovium, specified type NEC;
    • tapetoretinal - See: Dystrophy, retina;
    • thymus (gland) - E32.8 Other diseases of thymus
      • fatty - E32.8 Other diseases of thymus
    • thyroid (gland) - E07.89 Other specified disorders of thyroid
    • tricuspid (heart) (valve) - I07.9 Rheumatic tricuspid valve disease, unspecified
    • tuberculous NEC - See: Tuberculosis;
    • turbinate - J34.89 Other specified disorders of nose and nasal sinuses
    • uterus (cystic) - N85.8 Other specified noninflammatory disorders of uterus
    • vascular (senile) - See: Arteriosclerosis;
      • hypertensive - See: Hypertension;
    • vitreoretinal, secondary - See: Degeneration, retina, peripheral, secondary, vitreoretinal;
    • vitreous (body) - H43.81 Vitreous degeneration
    • Wallerian - See: Disorder, nerve;
    • Wilson's hepatolenticular - E83.01 Wilson's disease