hereditary diffuse leukoencephalopathy with spheroids

Preferred Label : hereditary diffuse leukoencephalopathy with spheroids;

MeSH synonym : neuroaxonal leukodystrophy; hereditary diffuse leukoencephalopathy with axonal spheroids; Adult-Onset leukodystrophy with neuroaxonal spheroids; autosomal dominant leukoencephalopathy with neuroaxonal spheroids; Gliosis, Familial Progressive Subcortical; Dementia, Familial, Neumann Type; Subcortical Gliosis of Neumann; Leukoencephalopathy, Diffuse Hereditary, With Spheroids; Leukoencephalopathy with Neuroaxonal Spheroids, Autosomal Dominant;

Is substance : O;

Details

Origin ID

C580150;

UMLS CUI

C3711381;

Automatic exact mappings (from CISMeF team)
- Adult-onset leukodystrophy with axonal spheroids [ICD-11 More detail]
- Neuroaxonal leukodystrophy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia [NCIt concept]
- Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia [ORDO Disease]
- Hereditary diffuse leukoencephalopathy with spheroids (disorder) [SNOMED CT concept]
- Leukoencephalopathy, hereditary diffuse, with spheroids [OMIM phenotypic series]
- adult-onset leukoencephalopathy with axonal spheroids and pigmented glia [DO Concept]
- hereditary diffuse leukoencephalopathy with spheroids [Disease (Nov.)]
MeSH term(s) associated for indexing
- leukoencephalopathies [MeSH Descriptor]
Record concept(s)
- hereditary diffuse leukoencephalopathy with spheroids [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia [NCIt concept]
- Hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia [ORDO Disease]
- Hereditary diffuse leukoencephalopathy with spheroids (disorder) [SNOMED CT concept]
- Leukoencephalopathy, hereditary diffuse, with spheroids 1 [OMIM Phenotype]
- hereditary diffuse leukoencephalopathy with spheroids [Disease (Nov.)]
Validated automatic mappings to BTNT
- Leukoencephalopathy, hereditary diffuse, with spheroids 1 [OMIM Phenotype]

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