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Leukoencephalopathy 22811006 SNOMED CT code SNOMED code 22811006 name Leukoencephalopathy status active date introduced 2002-01-31 fully specified name(s) Leukoencephalopathy (disorder) synonyms Leucoencephalopathy Leukoencephalopathy attributes - group1 Finding site Cerebral white matter structure 68523003 parents children Abscess of corpus callosum 735556002 Acute hemorrhagic leukoencephalitis 72986009 Atrophy of corpus callosum 253142006 Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome 771476007 Autosomal recessive spastic ataxia with leukoencephalopathy 784343003 Cathepsin A-related arteriopathy, strokes, leukoencephalopathy 1197429000 CLCN2-related leukoencephalopathy 768663003 COL4A1-related familial vascular leukoencephalopathy 778060000 Congenital malformation of corpus callosum 204042007 Corpus callosum syndrome 34184002 Cystic leukoencephalopathy without megalencephaly 720825005 Delayed post-hypoxic leukoencephalopathy 1259588007 Early-onset calcifying leukoencephalopathy, skeletal dysplasia 1222661007 Ectopic gray matter in centrum ovale 54794009 External capsule hemorrhage 195167002 Hereditary diffuse leukoencephalopathy with spheroids 702427005 Hypomyelination and congenital cataract 702379005 Internal capsule hemorrhage 52201006 Leukoencephalopathy co-occurrent with bilateral anterior temporal lobe cysts 719403003 Leukoencephalopathy due to copper deficiency 1186819005 Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome 735421004 Leukoencephalopathy with calcifications and cysts 1186710001 Leukoencephalopathy with metaphyseal chondrodysplasia syndrome 719405005 Leukoencephalopathy, dystonia, motor neuropathy syndrome 733452000 Leukoencephalopathy, palmoplantar keratoderma syndrome 771184001 Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome 763366000 Malignant neoplasm of corpus callosum 188301005 Megalencephalic leukoencephalopathy with subcortical cysts 703536004 Mitochondrial neurogastrointestinal encephalomyopathy syndrome 718214007 Neuroaxonal leukodystrophy 230367007 Optic radiation disorder 230521006 Pai syndrome 722201004 Perinatal periventricular hemorrhage 276649005 Periventricular hemorrhagic venous infarct 384993003 Periventricular leukomalacia 230769007 PLAA-associated neurodevelopmental disorder 1217367007 Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 702347001 Pontine autosomal dominant microangiopathy with leukoencephalopathy 1173997008 Posterior reversible encephalopathy syndrome 450886002 Progressive cavitating leukoencephalopathy 719267003 PYCR2-related microcephaly, progressive leukoencephalopathy 1237421000 Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 783787000 Toxic leukoencephalopathy 722602003 Traumatic hemorrhage of cerebral white matter 722630003 Vanishing white matter disease 447351004 White matter disease 16058431000119104 White matter disorder caused by infection 722601005 White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 724779000 White matter disorder due to vascular abnormality 737229001 White matter disorder due to vitamin B12 deficiency 762297005 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 118254002 406122000 298364001 22811006 138875005 404684003 246556002 299718000 81308009 22811006 ancestors sorted most to least specific
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