leukoencephalopathies

Preferred Label : leukoencephalopathies;

MeSH definition : Any of various diseases affecting the white matter of the central nervous system.;

MeSH synonym : leukoencephalopathy; white matter diseases; white matter disease;

CISMeF synonym : CACH/VWM syndrome; CACH/VWM syndromes; syndrome, CACH/VWM; syndromes, CACH/VWM; disease, white matter; diseases, white matter;

MeSH hyponym : Cree Leukoencephalopathy; Cree Leukoencephalopathies; Leukoencephalopathy, Cree; Leukoencephalopathy VWM5;

Related MeSH term : childhood ataxia with central nervous system hypomyelinization; Leukoencephalopathy with Vanishing White Matter; Childhood Ataxia with Diffuse Central Nervous System Hypomyelination; Vanishing White Matter Leukodystrophy; Cree Leukoencephalopathy; Cree Leukoencephalopathies; Leukoencephalopathies, Cree; Leukoencephalopathy, Cree; Childhood Ataxia with Central Nervous System Hypomyelination; CACH Syndrome; CACH Syndromes; Syndrome, CACH; Syndromes, CACH; Myelinosis Centralis Diffusa; Centralis Diffusa, Myelinosis; Centralis Diffusas, Myelinosis; Diffusa, Myelinosis Centralis; Diffusas, Myelinosis Centralis; Myelinosis Centralis Diffusas; CACH VWM Syndrome; CACH VWM Syndromes; Syndrome, CACH VWM; Syndromes, CACH VWM; VWM Syndrome, CACH; VWM Syndromes, CACH; Vanishing White Matter Disease; Leukoencephalopathy With Vanishing White Matter 1; Leukoencephalopathy VWM1;

Wikipedia link : https://en.wikipedia.org/wiki/Vanishing white matter leukodystrophy;

Details

Origin ID

D056784;

UMLS CUI

C0270612;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- CACH syndrome [ORDO Disease]
- CACH syndrome [ICD-11 More detail]
- Cree leukoencephalopathy [ORDO Disease]
- Leukoencephalopathy with Vanishing White Matter [NCIt concept]
- Leukoencephalopathy with vanishing white matter 1 [OMIM Phenotype]
- Vanishing white matter disease (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Leucoencephalopathy [PASCAL descriptor]
- Leukoencephalopathy [MedDRA Preferred Term]
- Leukoencephalopathy [HPO term]
- Leukoencephalopathy [NCIt concept]
- Leukoencephalopathy (disorder) [SNOMED CT concept]
- White matter disease (disorder) [SNOMED CT concept]
- leukencephalopathy [Disease (Nov.)]
- leukoencephalopathy, nos [SNOMED Notion]
HPO term
- Leukoencephalopathy [HPO term]
Record concept(s)
- Leukoencephalopathy With Vanishing White Matter 5 [MeSH concept]
- childhood ataxia with central nervous system hypomyelinization [MeSH concept]
- leukoencephalopathies [MeSH concept]
Related MeSH Supplementary Concept(s)
- Leukoencephalopathy Brain Calcifications and Cysts [MeSH Supplementary Concept]
- ataxia, spastic, 3, autosomal recessive [MeSH Supplementary Concept]
- cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy [MeSH Supplementary Concept]
- cerebroretinal microangiopathy with calcifications and cysts [MeSH Supplementary Concept]
- hereditary diffuse leukoencephalopathy with spheroids [MeSH Supplementary Concept]
- leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism [MeSH Supplementary Concept]
- leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation [MeSH Supplementary Concept]
- leukoencephalopathy with dystonia and motor neuropathy, SCPx-Deficient [MeSH Supplementary Concept]
- leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema [MeSH Supplementary Concept]
- leukoencephalopathy, arthritis, colitis, and hypogammaglobulinemia [MeSH Supplementary Concept]
- leukoencephalopathy, cystic, without megalencephaly [MeSH Supplementary Concept]
- muscular dystrophy, Adult-Onset, with leukoencephalopathy [MeSH Supplementary Concept]
- ribose 5-Phosphate isomerase deficiency [MeSH Supplementary Concept]
- telencephalic leukoencephalopathy [MeSH Supplementary Concept]
- vanishing white matter leukodystrophy with ovarian failure [MeSH Supplementary Concept]
See also
- White Matter [MeSH Descriptor]
- eukaryotic initiation Factor-2B [MeSH Descriptor]
See also inter- (CISMeF)
- Leukoencephalopathy, CTCAE [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Leukoencephalopathy [MedDRA Preferred Term]
- Leukoencephalopathy [HPO term]
- Leukoencephalopathy [NCIt concept]
- Leukoencephalopathy (disorder) [SNOMED CT concept]
- White matter disease (disorder) [SNOMED CT concept]
- leukencephalopathy [Disease (Nov.)]
- leukoencephalopathy, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- CACH syndrome [ORDO Disease]
- Cree leukoencephalopathy [ICD-11 More detail]
- leukoencephalopathy with vanishing white matter [DO Concept]
- leukoencephalopathy with vanishing white matter [Disease (Nov.)]

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