Disease
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Degenerative disorder (disorder)
Degenerative disorder
degeneratieve aandoening
Id362975008
StatusDefined
Associated morphologyDegenerative abnormality
ICD-10 complex map reference set
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified
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Acquired atrophy of fallopian tube1
Acquired atrophy of ovary1
Acquired atrophy of uterus
Acquired hypoganglionosis of large intestine
Acyl-CoA oxidase deficiency
Amelogenesis imperfecta, pigmented hypomaturation type
Amnion nodosum
Amyloidosis20
Amyotrophic lateral sclerosis type 12
Amyotrophic lateral sclerosis type 10
Amyotrophic lateral sclerosis type 3
Amyotrophic lateral sclerosis type 6
Amyotrophic lateral sclerosis type 7
Amyotrophic lateral sclerosis type 8
Amyotrophic lateral sclerosis type 9
Application site atrophy
Arthritis mutilans1
Atrophic endometrium1
Atrophic fibrosis of lung
Atrophic gastritis3
Atrophic rhinitis1
Atrophic surgical scar
Atrophic thrush1
Atrophic vulva
Atrophy of biliary tree2
Atrophy of breast
Atrophy of cervix1
Atrophy of gums1
Atrophy of kidney3
Atrophy of lacrimal gland3
Atrophy of liver2
Atrophy of multiple endocrine glands
Atrophy of nasal turbinates
Atrophy of orbital structure1
Atrophy of pancreas1
Atrophy of penis1
Atrophy of prostate1
Atrophy of salivary gland3
Atrophy of scrotum
Atrophy of seminal vesicle
Atrophy of spermatic cord1
Atrophy of testis3
Atrophy of thymus gland
Atrophy of tongue3
Atrophy of vagina1
Atrophy of vocal cord1
Calcinosis74
Carcinoid heart disease
Charcot-Marie-Tooth disease, type II4
Cholesterolosis of gallbladder
Chronic degenerative aortic valve disease
Chronic plaque-like oral candidiasis
Congenital degeneration of nervous system17
Congenital syphilitic mucous patches
Coronary arteriosclerosis in artery of transplanted heart
Cystic degeneration of lacrimal gland
Deafmutism-retinal degeneration syndrome
Degeneration of acoustic nerve
Degeneration of adrenal gland2
Degeneration of uterine fibroid
Degenerative disease of the central nervous system25
Degenerative disorder of ear5
Degenerative disorder of extremity
Degenerative disorder of eye30
Degenerative disorder of head
Degenerative disorder of muscle10
Degenerative disorder of musculoskeletal system28
Degenerative disorder of urethra2
Degenerative disorders of eyelids and periocular area4
Degenerative mitral valve prolapse
Degenerative myopia of left eye1
Degenerative myopia of right eye1
Degenerative progressive high myopia3
Degenerative sequelae of disorders40
Degenerative skin disorder28
Degenerative tear of triangular fibrocartilage complex of wrist2
Demineralization of tooth3
Deposition of excess fat on visceral pericardium
Drug-induced pigmentation5
Dubin-Johnson syndrome
Dying back phenomenon
Dystrophia unguium28
Dystrophy of multiple endocrine glands
Dystrophy of vulva1
Endocardial fibroelastosis4
Erosive pustular dermatosis1
Facial hemiatrophy1
Familial acantholysis
Familial visceral neuropathy2
Fibrocystic renal degeneration
Fibrous obliteration of appendix
Fragile X associated tremor ataxia syndrome
Gastric xanthelasma
Glomerulosclerosis7
Hemiatrophy of lower limb
Hemidystonia hemiatrophy syndrome
Hemiparkinsonism hemiatrophy syndrome
Hydropic degeneration of chorionic villi
Hyperemesis gravidarum before end of 22 week gestation with carbohydrate depletion
Hypoganglionosis
Idiopathic pleuroparenchymal fibroelastosis
IgA nephropathy2
Inhalation injury due to particulate matter
Injection site atrophy
Juvenile hemochromatosis2
Juvenile osteochondrosis of hand2
Kidney crystallization
Laser-induced hyperpigmentation
Lipoatrophy6
Lipodystrophy15
Local exogenous pigmentation of oral soft tissue1
Macerated fetus
Maleformatio ectodermalis generalisata of Bafverstedt
Mee's line
Melanosis20
Menkes kinky-hair syndrome
Metallosis5
Morton's metatarsalgia2
Motor neuropathy with multiple conduction block
Mucous patch of oral mucosa
Myocardial degeneration3
Myotubular myopathy with type I atrophy
Myxoid transformation of cardiac valve5
Neuronal ceroid lipofuscinosis6
Nutritional muscular degeneration
Obliteration of lymphatic vessel
Onychoatrophy4
Ossification anomaly with psychomotor developmental delay syndrome
Oxalate nephropathy
Pachyonychia congenita syndrome2
Panniculitis due to hyperuricemia
Papillary muscle degeneration1
Parenchymatous degeneration of liver
Pathological resorption of tooth5
Pemphigus8
Perforating dermatosis3
Peripheral demyelinating neuropathy9
Pigmented oral mucosal lesion5
Placenta fenestrata
Pneumoconiosis9
Polypoid degeneration of vocal cord
Polypoid sinus degeneration
Progressive muscular atrophy2
Proteinosis3
Pseudoxanthoma elasticum3
Pulp degeneration2
Sarcoidosis, plaque type
Schistosomal pigment deposition
Senile dermatosis4
Severe systemic illness-induced intestinal villous atrophy
Splenic atrophy
Steatosis6
Thyroid degeneration2
Tophus4
Tracheo-bronchial malacia in neonate
Transfusion reaction due to serum protein reaction1
Tropical ataxic neuropathy
Vascular degeneration14
Verruciform xanthoma of oral mucous membrane
Volume depletion, extrarenal loss
Volume depletion, gastrointestinal loss
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome
X-linked neurodegenerative syndrome Bertini type
X-linked neurodegenerative syndrome Hamel type
Xanthoma of lung