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Basilar white matter of pons
Cerebral white matter
White matter disorder caused by toxin
White matter necrosis

Translation of "White matter necrosis " (English → Dutch) :

White matter necrosis
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periventriculaire leukomalacie
SNOMEDCT-BE (disorder) / 230769007
SNOMEDCT-BE (disorder) / 230769007
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https://browser.ihtsdotools.or (...) [HTML]
Syndrome that has characteristics of severe antenatal microencephaly, simplified gyration, agenesis of the corpus callosum, absence of basal ganglia (very rare), pontocerebellar atrophy and involvement of the white matter with secondary cerebral atro
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primordiale dwerggroei met microcefalie door deficiëntie van 'zinc finger protein'-335
SNOMEDCT-NL (very rare), pontocerebellar atrophy and involvement of the white matter with secondary cerebral atro / 724141003
SNOMEDCT-NL (aandoening) / 724141003
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic neurological disorder defined by early-onset of neurologic symptoms, biphasic clinical course, unique MRI features (including extensive, symmetrical, deep white matter abnormalities), and increased lactate in body fluids. The severe fo
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leuko-encefalopathie, thalamus- en hersenstamanomalieën, hoog lactaatgehalte-syndroom
SNOMEDCT-BE (including extensive, symmetrical, deep white matter abnormalities), and increased lactate in body fluids. The severe fo / 763366000
SNOMEDCT-BE (disorder) / 763366000
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https://browser.ihtsdotools.or (...) [HTML]
A disorder of the white matter of the brain causing neurological problems, which can occur, anytime from childhood to adulthood. Characteristics of the disease include learning disabilities, retinopathy, atrophy of the optic nerves, spasticity, infer
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leuko-encefalopathie met milde cerebellaire ataxie en oedeem van witte materie
SNOMEDCT-BE (disorder) / 768663003
SNOMEDCT-BE (disorder) / 768663003
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic leukodystrophy disorder with characteristics of diffuse hypomyelination in the supratentorial brain white matter, brain stem and spinal cord. Patients usually present nystagmus, lower limb spasticity, hypotonia and motor developmental
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hypomyelinisatie met betrokkenheid van hersenstam en ruggenmerg en beenspasticiteit
SNOMEDCT-BE (disorder) / 777999008
SNOMEDCT-BE (disorder) / 777999008
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https://browser.ihtsdotools.or (...) [HTML]
This disease has characteristics of progressive cerebellar ataxia with pyramidal and spinal cord dysfunction, associated with distinctive MRI anomalies and increased lactate in the abnormal white matter. Onset occurs in early childhood. Epilepsy and
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leuko-encefalopathie met betrokkenheid van hersenstam en ruggenmerg, hoog lactaatgehalte-syndroom
SNOMEDCT-BE (disorder) / 735421004
SNOMEDCT-BE (disorder) / 735421004
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https://browser.ihtsdotools.or (...) [HTML]
Cerebral white matter
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gehele witte stof van hersenen
SNOMEDCT-NL (lichaamsstructuur) / 361691006
SNOMEDCT-NL (lichaamsstructuur) / 361691006
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https://browser.ihtsdotools.or (...) [HTML]
White matter disorder caused by toxin
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wittestofafwijking door toxine
SNOMEDCT-NL (aandoening) / 722602003
SNOMEDCT-NL (aandoening) / 722602003
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https://browser.ihtsdotools.or (...) [HTML]
Basilar white matter of pons
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structuur van substantia alba van pars basilaris pontis
SNOMEDCT-NL (lichaamsstructuur) / 16048002
SNOMEDCT-NL (lichaamsstructuur) / 16048002
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https://browser.ihtsdotools.or (...) [HTML]
A rare neuroinflammatory disease characterized by the onset of ataxia, dysarthria and cerebral white matter changes that are triggered by viral infection. Episodic progressive neurodegeneration (manifesting with loss of motor and verbal skills, muscl
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fatale post-virale neurogeneratieve stoornis
SNOMEDCT-BE (manifesting with loss of motor and verbal skills, muscl / 774206008
SNOMEDCT-BE (disorder) / 774206008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


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'White matter necrosis'

Date index:2023-03-19 -

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