Multiple Sclerosis

Preferred Label : Multiple Sclerosis;

NCIt definition : A progressive autoimmune disorder affecting the central nervous system resulting in demyelination. Patients develop physical and cognitive impairments that correspond with the affected nerve fibers.;

Alternative definition : NICHD: An autoimmune demyelinating disease characterized by a relapsing-remitting or progressive pattern of central nervous system impairment.; NCI-GLOSS: A disorder of the central nervous system marked by weakness, numbness, a loss of muscle coordination, and problems with vision, speech, and bladder control. Multiple sclerosis is thought to be an autoimmune disease in which the body's immune system destroys myelin. Myelin is a substance that contains both protein and fat (lipid), serving as a nerve insulator and helping in the transmission of nerve signals.;

Codes from synonyms : CDR0000044135; G35;

Details

Origin ID

C3243;

UMLS CUI

C0026769;

Currated CISMeF NLP mapping
- Multiple sclerosis [PASCAL descriptor]
- Multiple sclerosis [LOINC component]
- Multiple sclerosis [ICD-10 category]
- Multiple sclerosis [ICD-9 code]
- Multiple sclerosis [ICD-11 Category]
- Multiple sclerosis [HPMULTI term]
- Multiple sclerosis [ICD-10 category (who)]
- Multiple sclerosis [MedDRA Preferred Term]
- Multiple sclerosis [ORDO Disease]
- Multiple sclerosis (disorder) [SNOMED CT concept]
- Multiple sclerosis, susceptibility to [OMIM Phenotype]
- Sclerosis multiple [MedDRA LLT]
- multiple sclerosis [DO Concept]
- multiple sclerosis [Disease (Nov.)]
- multiple sclerosis [COVID-19 Thesaurus concept]
- multiple sclerosis [ICPC-2 Rubric]
- multiple sclerosis [DRC Consultation result]
- multiple sclerosis [MedlinePlus Topic]
- multiple sclerosis [MeSH Descriptor]
- multiple sclerosis [MeSH concept]
- multiple sclerosis [Radlex concept]
- multiple sclerosis, nos [SNOMED Notion]
DO Cross reference
- multiple sclerosis [DO Concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disseminated sclerosis [MedDRA LLT]
- Generalized multiple sclerosis (disorder) [SNOMED CT concept]
- Multiple sclerosis [ORDO Disease]
- Multiple sclerosis [ICD-9 code]
- Multiple sclerosis [LOINC component]
- Multiple sclerosis [ICD-10 category]
- Multiple sclerosis [ICD-10 category (who)]
- Multiple sclerosis [MedDRA Preferred Term]
- Multiple sclerosis (disorder) [SNOMED CT concept]
- Sclerosis multiple [MedDRA LLT]
- multiple sclerosis [DRC Consultation result]
- multiple sclerosis [DO Concept]
- multiple sclerosis [ICPC-2 Rubric]
- multiple sclerosis [MeSH concept]
- multiple sclerosis [MedlinePlus Topic]
- multiple sclerosis [MeSH Descriptor]
- multiple sclerosis, nos [SNOMED Notion]
associated_with_malfunction_of_gene_product
- Interleukin-17A [NCIt concept]
- Receptor-Type Tyrosine-Protein Phosphatase C [NCIt concept]
concept_is_in_subset
- CPTAC Codelists Terminology [NCIt concept]
- CPTAC Medical Conditions Codelist [NCIt concept]
- CPTAC Terminology [NCIt concept]
- CTRP Disease Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
- HL Authorized Value Terminology [NCIt concept]
- HL Medical History Table [NCIt concept]
- NICHD Terminology [NCIt concept]
- Pediatric Adverse Events Terminology [NCIt concept]
- Pediatric Adverse Events Terminology Mapped to MedDRA [NCIt concept]
- mCode Elixhauser Other Neurological Disorder Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_associated_gene
- IL17A Gene [NCIt concept]
- IL17A wt Allele [NCIt concept]
- PTPRC Gene [NCIt concept]
- PTPRC wt Allele [NCIt concept]
- TAP2 Gene [NCIt concept]
- TAP2 wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

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