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Alcoholic cerebellar ataxia
Angioid streaks
Cerebral degeneration
Cerebral degeneration due to Creutzfeldt-Jakob disease
Cyst
Degeneration
Dementia in cerebral lipidosis
Drusen
Dysfunction of autonomic nervous system due to alcohol
Encephalopathy
Epilepsy
Hepatolenticular degeneration
Hole
Hypercalcaemia
Intoxications
Multiple sclerosis
Neurosyphilis
Niacin deficiency
Of macula
Pellagra
Polyarteritis nodosa
Puckering
Systemic lupus erythematosus
Vitamin B12 deficiency

Translation of "Cerebral degeneration " (English → Dutch) :

Cerebral degeneration due to Creutzfeldt-Jakob disease
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cerebrale degeneratie door subacute spongiforme encefalopathie
SNOMEDCT-NL (aandoening) / 192818008
SNOMEDCT-NL (aandoening) / 192818008
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https://browser.ihtsdotools.or (...) [HTML]
Cerebral degeneration
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degeneratieve hersenaandoening
SNOMEDCT-BE (disorder) / 52522001
SNOMEDCT-BE (disorder) / 52522001
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https://browser.ihtsdotools.or (...) [HTML]
Alcoholic:cerebellar:ataxia | degeneration | cerebral degeneration | encephalopathy | Dysfunction of autonomic nervous system due to alcohol
https://icd.who.int/browse10/2 (...) (...) [HTML]
alcoholische | cerebellaire | ataxie | alcoholische | cerebellaire | degeneratie | alcoholische | cerebrale degeneratie | alcoholische | encefalopathie | disfunctie van autonoom zenuwstelsel door alcoholgebruik
WORLD HEALTH ORGANIZATION ICD-10: G31.2
WORLD HEALTH ORGANIZATION ICD-10: G31.2
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://terminologie.nictiz.nl (...) [HTML]
Dementia in:cerebral lipidosis (E75.-+) | epilepsy (G40.-+) | hepatolenticular degeneration (E83.0+) | hypercalcaemia (E83.5+) | hypothyroidism, acquired (E01.-+, E03.-+) | intoxications (T36-T65+) | multiple sclerosis (G35+) | neurosyphilis (A52.1+) | niacin deficiency [pellagra] (E52+) | polyarteritis nodosa (M30.0+) | systemic lupus erythematosus (M32.-+) | trypanosomiasis (B56.-+, B57.-+) | vitamin B12 deficiency (E53.8+)
https://icd.who.int/browse10/2 (...) (...) [HTML]
dementie bij | epilepsie (G40.-) | dementie bij | hepatolenticulaire degeneratie (E83.0) | dementie bij | hersenlipidose (E75.-) | dementie bij | hypercalciëmie (E83.5) | dementie bij | hypothyroïdie, verworven (E01.-, E03.-) | dementie bij | intoxicaties (T36-T65) | dementie bij | lupus erythematodes disseminatus (M32.-) | dementie bij | multipele sclerose (G35) | dementie bij | neurosyfilis (A52.1) | dementie bij | niacinedeficiëntie [pellagra] (E52) | dementie bij | polyarteriitis nodosa (M30.0) | dementie bij | trypanosomiasis (B56.-, B57.-) | dementie bij | uremie (N18.5) | dementie bij | vitamine B12-deficiëntie (E53.8)
WORLD HEALTH ORGANIZATION ICD-10: F02.8*
WORLD HEALTH ORGANIZATION ICD-10: F02.8*
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://terminologie.nictiz.nl (...) [HTML]
Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
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spinocerebellaire ataxie type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008
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https://browser.ihtsdotools.or (...) [HTML]
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies
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autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type D
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies / 765747004
SNOMEDCT-BE (disorder) / 765747004
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https://browser.ihtsdotools.or (...) [HTML]
Angioid streaks | Cyst | Drusen (degenerative) | Hole | Puckering | of macula | Kuhnt-Junius degeneration Senile macular degeneration (atrophic)(exudative) Toxic maculopathy
https://icd.who.int/browse10/2 (...) (...) [HTML]
angioïde strepenvan macula | cystevan macula | drusen (degeneratief)van macula | gatvan macula | macular pucker | Kuhnt-Junius-degeneratie | seniele maculadegeneratie (atrofisch)(exsudatief) | toxische maculopathie
WORLD HEALTH ORGANIZATION ICD-10: H35.3
WORLD HEALTH ORGANIZATION ICD-10: H35.3
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://terminologie.nictiz.nl (...) [HTML]
Syndrome with characteristics of progressive pigmentary retinal degeneration (with nyctalopia and visual field restriction), cystic macular degeneration and angle closure glaucoma. It has been described in seven members of one family. Patients also h
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syndroom van retinadegeneratie, nanophthalmos en glaucoom
SNOMEDCT-NL / 723503006
SNOMEDCT-NL (aandoening) / 723503006
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https://browser.ihtsdotools.or (...) [HTML]
A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl
https://browser.ihtsdotools.or (...) (...) [HTML]
autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m
https://browser.ihtsdotools.or (...) (...) [HTML]
autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type B
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with m / 765745007
SNOMEDCT-BE (disorder) / 765745007
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : angioid streaks    cerebral degeneration    drusen    puckering    degeneration    encephalopathy    epilepsy    hepatolenticular degeneration    hypercalcaemia    intoxications    multiple sclerosis    neurosyphilis    niacin deficiency    macula    pellagra    polyarteritis nodosa    systemic lupus erythematosus    trypanosomiasis    vitamin b12 deficiency    Cerebral degeneration    


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'Cerebral degeneration'

Date index:2023-02-27 -

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