Multifocal Fibrosclerosis

Preferred Label : Multifocal Fibrosclerosis;

NCIt definition : A rare syndrome of unknown etiology characterized by progressive fibrosis involving multiple organ sites.;

Codes from synonyms : M35.5;

Details

Origin ID

C197936;

UMLS CUI

C0494949;

Automatic exact mappings (from CISMeF team)
- Fibrosclerosis, multifocal [OMIM Phenotype]
Currated CISMeF NLP mapping
- Multifocal fibrosclerosis [MeSH concept]
- Multifocal fibrosclerosis [ICD-10 Sub-category]
- Multifocal fibrosclerosis [MedDRA Preferred Term]
- Multifocal fibrosclerosis [ICD-11 More detail]
- Multifocal fibrosclerosis [PASCAL descriptor]
- Multifocal fibrosclerosis [ICD-10 Sub-category (who)]
- Multifocal fibrosclerosis (disorder) [SNOMED CT concept]
- multifocal fibrosclerosis [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Fibrosclerosis, multifocal [OMIM Phenotype]
- Multifocal fibrosclerosis [MeSH concept]
- Multifocal fibrosclerosis [MedDRA Preferred Term]
- Multifocal fibrosclerosis [ICD-10 Sub-category]
- Multifocal fibrosclerosis (disorder) [SNOMED CT concept]
- multifocal fibrosclerosis [MeSH Supplementary Concept]
concept_is_in_subset
- mCode Elixhauser Rheumatoid Arthritis and Collagen Vascular Disease Value Set [NCIt concept]
- mCode Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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