amyotrophic lateral sclerosis 6, autosomal recessive

Preferred Label : amyotrophic lateral sclerosis 6, autosomal recessive;

MeSH note : mutations in FUS;

Origin ID

C567699;

UMLS CUI

C2750729;

Currated CISMeF NLP mapping
- Amyotrophic Lateral Sclerosis 6, With or Without Frontotemporal Dementia [NCIt concept]
- Amyotrophic lateral sclerosis 6 with or without frontotemporal dementia [OMIM Phenotype]
- amyotrophic lateral sclerosis type 6 [DO Concept]
MeSH term(s) associated for indexing
- amyotrophic lateral sclerosis [MeSH Descriptor]
- frontotemporal dementia [MeSH Descriptor]
Record concept(s)
- amyotrophic lateral sclerosis 6, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to NTBT
- Amyotrophic lateral sclerosis type 6 (disorder) [SNOMED CT concept]