Atrophy, atrophic (of)

"Atrophy, atrophic (of)" 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 "atrophy, atrophic (of)"

Atrophy, atrophic (of)
- adrenal (capsule) (gland) - E27.49 Other adrenocortical insufficiency
  - primary (autoimmune) - E27.1 Primary adrenocortical insufficiency
- alveolar process or ridge (edentulous) - K08.20 Unspecified atrophy of edentulous alveolar ridge
- anal sphincter (disuse) - N81.84 Pelvic muscle wasting
- appendix - K38.8 Other specified diseases of appendix
- arteriosclerotic - See: Arteriosclerosis;
- bile duct (common) (hepatic) - K83.8 Other specified diseases of biliary tract
- bladder - N32.89 Other specified disorders of bladder
  - neurogenic - N31.8 Other neuromuscular dysfunction of bladder
- blanche (en plaque) (of Milian) - L95.0 Livedoid vasculitis
- bone (senile) NEC - See Also: Disorder, bone, specified type NEC;
  - due to
    - tabes dorsalis (neurogenic) - A52.11 Tabes dorsalis
- brain (cortex) (progressive) - G31.9 Degenerative disease of nervous system, unspecified
  - frontotemporal circumscribed - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
    - with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G31.01 Pick's disease
  - senile NEC - G31.1 Senile degeneration of brain, not elsewhere classified
- breast - N64.2 Atrophy of breast
  - obstetric - See: Disorder, breast, specified type NEC;
- buccal cavity - K13.79 Other lesions of oral mucosa
- cardiac - See: Degeneration, myocardial;
- cartilage (infectional) (joint) - See: Disorder, cartilage, specified NEC;
- cerebellar - See: Atrophy, brain;
- cerebral - See: Atrophy, brain;
- cervix (mucosa) (senile) (uteri) - N88.8 Other specified noninflammatory disorders of cervix uteri
  - menopausal - N95.8 Other specified menopausal and perimenopausal disorders
- Charcot-Marie-Tooth - G60.0 Hereditary motor and sensory neuropathy
- choroid (central) (macular) (myopic) (retina) - H31.10 Unspecified choroidal degeneration
  - diffuse secondary - H31.12 Diffuse secondary atrophy of choroid
  - gyrate - H31.23 Gyrate atrophy, choroid
  - senile - H31.11 Age-related choroidal atrophy
- ciliary body - See: Atrophy, iris;
- conjunctiva (senile) - H11.89 Other specified disorders of conjunctiva
- corpus cavernosum - N48.89 Other specified disorders of penis
- cortical - See: Atrophy, brain;
- cystic duct - K82.8 Other specified diseases of gallbladder
- Déjérine-Thomas - G23.8 Other specified degenerative diseases of basal ganglia
- disuse NEC - See: Atrophy, muscle;
- Duchenne-Aran - G12.21 Amyotrophic lateral sclerosis
- ear - H93.8 Other specified disorders of ear
- edentulous alveolar ridge - K08.20 Unspecified atrophy of edentulous alveolar ridge
- endometrium (senile) - N85.8 Other specified noninflammatory disorders of uterus
  - cervix - N88.8 Other specified noninflammatory disorders of cervix uteri
- enteric - K63.89 Other specified diseases of intestine
- epididymis - N50.89 Other specified disorders of the male genital organs
- eyeball - See: Disorder, globe, degenerated condition, atrophy;
- eyelid (senile) - See: Disorder, eyelid, degenerative;
- facial (skin) - L90.9 Atrophic disorder of skin, unspecified
- fallopian tube (senile) - N83.32 Acquired atrophy of fallopian tube
  - with ovary - N83.33 Acquired atrophy of ovary and fallopian tube
- fascioscapulohumeral (Landouzy- Déjérine) - G71.02 Facioscapulohumeral muscular dystrophy
- fatty, thymus (gland) - E32.8 Other diseases of thymus
- gallbladder - K82.8 Other specified diseases of gallbladder
- gastric - K29.40 Chronic atrophic gastritis without bleeding
  - with bleeding - K29.41 Chronic atrophic gastritis with bleeding
- gastrointestinal - K63.89 Other specified diseases of intestine
- glandular - I89.8 Other specified noninfective disorders of lymphatic vessels and lymph nodes
- globe - H44.52 Atrophy of globe
- gum - See: Recession, gingival;
- hair - L67.8 Other hair color and hair shaft abnormalities
- heart (brown) - See: Degeneration, myocardial;
- hemifacial - Q67.4 Other congenital deformities of skull, face and jaw
  - Romberg - G51.8 Other disorders of facial nerve
- infantile - E41 Nutritional marasmus
  - paralysis, acute - See: Poliomyelitis, paralytic;
- intestine - K63.89 Other specified diseases of intestine
- iris (essential) (progressive) - H21.26 Iris atrophy (essential) (progressive)
  - specified NEC - H21.29 Other iris atrophy
- kidney (senile) (terminal) - See Also: Sclerosis, renal; - N26.1 Atrophy of kidney (terminal)
  - congenital or infantile - Q60.5 Renal hypoplasia, unspecified
    - bilateral - Q60.4 Renal hypoplasia, bilateral
    - unilateral - Q60.3 Renal hypoplasia, unilateral
  - hydronephrotic - See: Hydronephrosis;
- lacrimal gland (primary) - H04.14 Primary lacrimal gland atrophy
  - secondary - H04.15 Secondary lacrimal gland atrophy
- Landouzy-Déjérine - G71.02 Facioscapulohumeral muscular dystrophy
- laryngitis, infective - J37.0 Chronic laryngitis
- larynx - J38.7 Other diseases of larynx
- Leber's optic (hereditary) - H47.22 Hereditary optic atrophy
- lip - K13.0 Diseases of lips
- liver (yellow) - K72.90 Hepatic failure, unspecified without coma
  - acute, subacute - K72.00 Acute and subacute hepatic failure without coma
    - with coma - K72.01 Acute and subacute hepatic failure with coma
  - chronic - K72.10 Chronic hepatic failure without coma
    - with coma - K72.11 Chronic hepatic failure with coma
  - with coma - K72.91 Hepatic failure, unspecified with coma
- lung (senile) - J98.4 Other disorders of lung
- macular (dermatological) - L90.8 Other atrophic disorders of skin
  - syphilitic, skin - A51.39 Other secondary syphilis of skin
    - striated - A52.79 Other symptomatic late syphilis
- mandible (edentulous) - K08.20 Unspecified atrophy of edentulous alveolar ridge
  - minimal - K08.21 Minimal atrophy of the mandible
  - moderate - K08.22 Moderate atrophy of the mandible
  - severe - K08.23 Severe atrophy of the mandible
- maxilla - K08.20 Unspecified atrophy of edentulous alveolar ridge
  - minimal - K08.24 Minimal atrophy of maxilla
  - moderate - K08.25 Moderate atrophy of the maxilla
  - severe - K08.26 Severe atrophy of the maxilla
- muscle, muscular (diffuse) (general) (idiopathic) (primary) - M62.50 Muscle wasting and atrophy, not elsewhere classified, unspecified site
  - ankle - M62.57 Muscle wasting and atrophy, not elsewhere classified, ankle and foot
  - back - M62.5A9 Muscle wasting and atrophy, not elsewhere classified, back, unspecified level
    - cervical - M62.5A0 Muscle wasting and atrophy, not elsewhere classified, back, cervical
    - lumbosacral - M62.5A2 Muscle wasting and atrophy, not elsewhere classified, back, lumbosacral
    - thoracic - M62.5A1 Muscle wasting and atrophy, not elsewhere classified, back, thoracic
  - Duchenne-Aran - G12.21 Amyotrophic lateral sclerosis
  - foot - M62.57 Muscle wasting and atrophy, not elsewhere classified, ankle and foot
  - forearm - M62.53 Muscle wasting and atrophy, not elsewhere classified, forearm
  - hand - M62.54 Muscle wasting and atrophy, not elsewhere classified, hand
  - infantile spinal - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
  - lower leg - M62.56 Muscle wasting and atrophy, not elsewhere classified, lower leg
  - multiple sites - M62.59 Muscle wasting and atrophy, not elsewhere classified, multiple sites
  - myelopathic - See: Atrophy, muscle, spinal;
  - myotonic - G71.11 Myotonic muscular dystrophy
  - neuritic - G58.9 Mononeuropathy, unspecified
  - neuropathic (peroneal) (progressive) - G60.0 Hereditary motor and sensory neuropathy
  - pelvic (disuse) - N81.84 Pelvic muscle wasting
  - peroneal - G60.0 Hereditary motor and sensory neuropathy
  - progressive (bulbar) - G12.21 Amyotrophic lateral sclerosis
    - adult - G12.1 Other inherited spinal muscular atrophy
    - infantile (spinal) - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
    - spinal - G12.25 Progressive spinal muscle atrophy
      - adult - G12.1 Other inherited spinal muscular atrophy
      - infantile - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
  - pseudohypertrophic - G71.02 Facioscapulohumeral muscular dystrophy
  - shoulder region - M62.51 Muscle wasting and atrophy, not elsewhere classified, shoulder
  - specified site NEC - M62.58 Muscle wasting and atrophy, not elsewhere classified, other site
  - spinal - G12.9 Spinal muscular atrophy, unspecified
    - adult form - G12.1 Other inherited spinal muscular atrophy
    - Aran-Duchenne - G12.21 Amyotrophic lateral sclerosis
    - childhood form, type II - G12.1 Other inherited spinal muscular atrophy
    - distal - G12.1 Other inherited spinal muscular atrophy
    - hereditary NEC - G12.1 Other inherited spinal muscular atrophy
    - infantile, type I (Werdnig-Hoffmann) - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
    - juvenile form, type III (Kugelberg- Welander) - G12.1 Other inherited spinal muscular atrophy
    - progressive - G12.25 Progressive spinal muscle atrophy
    - scapuloperoneal form - G12.1 Other inherited spinal muscular atrophy
    - specified NEC - G12.8 Other spinal muscular atrophies and related syndromes
  - syphilitic - A52.78 Syphilis of other musculoskeletal tissue
  - thigh - M62.55 Muscle wasting and atrophy, not elsewhere classified, thigh
  - upper arm - M62.52 Muscle wasting and atrophy, not elsewhere classified, upper arm
- myocardium - See: Degeneration, myocardial;
- myometrium (senile) - N85.8 Other specified noninflammatory disorders of uterus
  - cervix - N88.8 Other specified noninflammatory disorders of cervix uteri
- myopathic NEC - See: Atrophy, muscle;
- myotonia - G71.11 Myotonic muscular dystrophy
- nail - L60.3 Nail dystrophy
- nasopharynx - J31.1 Chronic nasopharyngitis
- nerve - See Also: Disorder, nerve;
  - abducens - See: Strabismus, paralytic, sixth nerve;
  - accessory - G52.8 Disorders of other specified cranial nerves
  - acoustic or auditory
  - cranial - G52.9 Cranial nerve disorder, unspecified
    - eighth (auditory)
    - eleventh (accessory) - G52.8 Disorders of other specified cranial nerves
    - fifth (trigeminal) - G50.8 Other disorders of trigeminal nerve
    - first (olfactory) - G52.0 Disorders of olfactory nerve
    - fourth (trochlear) - See: Strabismus, paralytic, fourth nerve;
    - second (optic) - H47.20 Unspecified optic atrophy
    - sixth (abducens) - See: Strabismus, paralytic, sixth nerve;
    - tenth (pneumogastric) (vagus) - G52.2 Disorders of vagus nerve
    - third (oculomotor) - See: Strabismus, paralytic, third nerve;
    - twelfth (hypoglossal) - G52.3 Disorders of hypoglossal nerve
  - hypoglossal - G52.3 Disorders of hypoglossal nerve
  - oculomotor - See: Strabismus, paralytic, third nerve;
  - olfactory - G52.0 Disorders of olfactory nerve
  - optic (papillomacular bundle)
    - syphilitic (late) - A52.15 Late syphilitic neuropathy
      - congenital - A50.44 Late congenital syphilitic optic nerve atrophy
  - pneumogastric - G52.2 Disorders of vagus nerve
  - trigeminal - G50.8 Other disorders of trigeminal nerve
  - trochlear - See: Strabismus, paralytic, fourth nerve;
  - vagus (pneumogastric) - G52.2 Disorders of vagus nerve
- neurogenic, bone, tabetic - A52.11 Tabes dorsalis
- nutritional - E43 Unspecified severe protein-calorie malnutrition
  - with marasmus - E41 Nutritional marasmus
- old age - R54 Age-related physical debility
- olivopontocerebellar - G23.8 Other specified degenerative diseases of basal ganglia
- optic (nerve) - H47.20 Unspecified optic atrophy
  - glaucomatous - H47.23 Glaucomatous optic atrophy
  - hereditary - H47.22 Hereditary optic atrophy
  - primary - H47.21 Primary optic atrophy
  - specified type NEC - H47.29 Other optic atrophy
  - syphilitic (late) - A52.15 Late syphilitic neuropathy
    - congenital - A50.44 Late congenital syphilitic optic nerve atrophy
- orbit - H05.31 Atrophy of orbit
- ovary (senile) - N83.31 Acquired atrophy of ovary
  - with fallopian tube - N83.33 Acquired atrophy of ovary and fallopian tube
- oviduct (senile) - See: Atrophy, fallopian tube;
- palsy, diffuse (progressive) - G12.22 Progressive bulbar palsy
- pancreas (duct) (senile) - K86.89 Other specified diseases of pancreas
- parotid gland - K11.0 Atrophy of salivary gland
- pelvic muscle - N81.84 Pelvic muscle wasting
- penis - N48.89 Other specified disorders of penis
- pharynx - J39.2 Other diseases of pharynx
- pluriglandular - E31.8 Other polyglandular dysfunction
  - autoimmune - E31.0 Autoimmune polyglandular failure
- polyarthritis - M15.9 Polyosteoarthritis, unspecified
- prostate - N42.89 Other specified disorders of prostate
- pseudohypertrophic (muscle) - G71.02 Facioscapulohumeral muscular dystrophy
- renal - See Also: Sclerosis, renal; - N26.1 Atrophy of kidney (terminal)
- retina, retinal (postinfectional) - H35.89 Other specified retinal disorders
- rhinitis - J31.0 Chronic rhinitis
- salivary gland - K11.0 Atrophy of salivary gland
- scar - L90.5 Scar conditions and fibrosis of skin
- sclerosis, lobar (of brain) - See Also: Dementia, in, diseases specified elsewhere; - G31.09 Other frontotemporal neurocognitive disorder
  - with behavioral disturbance - See Also: Dementia, in, diseases specified elsewhere; - G31.09 Other frontotemporal neurocognitive disorder
- scrotum - N50.89 Other specified disorders of the male genital organs
- seminal vesicle - N50.89 Other specified disorders of the male genital organs
- senile - R54 Age-related physical debility
  - due to radiation (nonionizing) (solar) - L57.8 Other skin changes due to chronic exposure to nonionizing radiation
- skin (patches) (spots) - L90.9 Atrophic disorder of skin, unspecified
  - degenerative (senile) - L90.8 Other atrophic disorders of skin
  - due to radiation (nonionizing) (solar) - L57.8 Other skin changes due to chronic exposure to nonionizing radiation
  - senile - L90.8 Other atrophic disorders of skin
- spermatic cord - N50.89 Other specified disorders of the male genital organs
- spinal (acute) (cord) - G95.89 Other specified diseases of spinal cord
  - muscular - See: Atrophy, muscle, spinal;
  - paralysis - G12.20 Motor neuron disease, unspecified
    - acute - See: Poliomyelitis, paralytic;
    - meaning progressive muscular atrophy - G12.25 Progressive spinal muscle atrophy
- spine (column) - See: Spondylopathy, specified NEC;
- spleen (senile) - D73.0 Hyposplenism
- stomach - K29.40 Chronic atrophic gastritis without bleeding
  - with bleeding - K29.41 Chronic atrophic gastritis with bleeding
- striate (skin) - L90.6 Striae atrophicae
  - syphilitic - A52.79 Other symptomatic late syphilis
- subcutaneous - L90.9 Atrophic disorder of skin, unspecified
- sublingual gland - K11.0 Atrophy of salivary gland
- submandibular gland - K11.0 Atrophy of salivary gland
- submaxillary gland - K11.0 Atrophy of salivary gland
- Sudeck's - See: Algoneurodystrophy;
- suprarenal (capsule) (gland) - E27.49 Other adrenocortical insufficiency
  - primary - E27.1 Primary adrenocortical insufficiency
- systemic affecting central nervous system
  - in
    - myxedema - E03.9 Hypothyroidism, unspecified
    - neoplastic disease - See Also: Neoplasm; - D49.9 Neoplasm of unspecified behavior of unspecified site
    - specified disease NEC - G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere
- tarso-orbital fascia, congenital - Q10.3 Other congenital malformations of eyelid
- testis - N50.0 Atrophy of testis
- thenar, partial - See: Syndrome, carpal tunnel;
- thymus (fatty) - E32.8 Other diseases of thymus
- thyroid (gland) (acquired) - E03.4 Atrophy of thyroid (acquired)
  - congenital (with myxedema) - E03.1 Congenital hypothyroidism without goiter
  - with cretinism - E03.1 Congenital hypothyroidism without goiter
- tongue (senile) - K14.8 Other diseases of tongue
  - papillae - K14.4 Atrophy of tongue papillae
- trachea - J39.8 Other specified diseases of upper respiratory tract
- tunica vaginalis - N50.89 Other specified disorders of the male genital organs
- turbinate - J34.89 Other specified disorders of nose and nasal sinuses
- tympanic membrane (nonflaccid) - H73.82 Atrophic nonflaccid tympanic membrane
  - flaccid - H73.81 Atrophic flaccid tympanic membrane
- upper respiratory tract - J39.8 Other specified diseases of upper respiratory tract
- uterus, uterine (senile) - N85.8 Other specified noninflammatory disorders of uterus
  - cervix - N88.8 Other specified noninflammatory disorders of cervix uteri
  - due to radiation (intended effect) - N85.8 Other specified noninflammatory disorders of uterus
    - adverse effect or misadventure - N99.89 Other postprocedural complications and disorders of genitourinary system
- vagina (senile) - N95.2 Postmenopausal atrophic vaginitis
- vas deferens - N50.89 Other specified disorders of the male genital organs
- vascular - I99.8 Other disorder of circulatory system
- vertebra (senile) - See: Spondylopathy, specified NEC;
- vulva (senile) - N90.5 Atrophy of vulva
- Werdnig-Hoffmann - G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
- yellow - See: Failure, hepatic;