amyotrophic lateral sclerosis 1

Preferred Label : amyotrophic lateral sclerosis 1;

CISMeF synonym : amyotrophic lateral sclerosis, familial;

MeSH synonym : amyotrophic lateral sclerosis, autosomal dominant;

Details

Origin ID

C531617;

UMLS CUI

C1862939;

Currated CISMeF NLP mapping
- Amyotrophic Lateral Sclerosis 1 [NCIt concept]
- Amyotrophic lateral sclerosis 1 [OMIM Phenotype]
- Amyotrophic lateral sclerosis type 1 (disorder) [SNOMED CT concept]
- Familial amyotrophic lateral sclerosis [MedDRA Preferred Term]
- amyotrophic lateral sclerosis type 1 [DO Concept]
- familial amyotrophic lateral sclerosis [Disease (Nov.)]
MeSH term(s) associated for indexing
- amyotrophic lateral sclerosis [MeSH Descriptor]
Record concept(s)
- Amyotrophic Lateral Sclerosis, Familial [MeSH concept]
- Amyotrophic lateral sclerosis 1 [MeSH concept]
- amyotrophic lateral sclerosis, sporadic [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyotrophic Lateral Sclerosis 1 [NCIt concept]
- Amyotrophic lateral sclerosis 1 [OMIM Phenotype]
- Amyotrophic lateral sclerosis type 1 (disorder) [SNOMED CT concept]
- amyotrophic lateral sclerosis type 1 [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients