amyotrophic lateral sclerosis 4, juvenile

Preferred Label : amyotrophic lateral sclerosis 4, juvenile;

MeSH synonym : neuronopathy, distal hereditary motor, with pyramidal features;

Origin ID

C566550;

UMLS CUI

C1865409;

Automatic exact mappings (from CISMeF team)
- amyotrophic lateral sclerosis type 4 [DO Concept]
Currated CISMeF NLP mapping
- Amyotrophic lateral sclerosis 4, juvenile [OMIM Phenotype]
MeSH term(s) associated for indexing
- amyotrophic lateral sclerosis [MeSH Descriptor]
Record concept(s)
- amyotrophic lateral sclerosis 4, juvenile [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyotrophic lateral sclerosis 4, juvenile [OMIM Phenotype]
- Amyotrophic lateral sclerosis type 4 [ORDO Disease]
- Amyotrophic lateral sclerosis type 4 (disorder) [SNOMED CT concept]