spinal muscular atrophies of childhood

Preferred Label : spinal muscular atrophies of childhood;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0022919;

UMLS CUI

C0700595;

Automatic exact mappings (from CISMeF team)
- Proximal spinal muscular atrophy type 1 [ORDO Disease]
- childhood spinal muscular atrophy [DO Concept]
- juvenile spinal muscular atrophy [DO Concept]
Currated CISMeF NLP mapping
- Spinal Muscular Atrophy of Childhood [NCIt concept]
- spinal muscular atrophies of childhood [Disease (Nov.)]
MeSH narrower concept(s)
- Muscular atrophy, spinal, infantile chronic form [MeSH concept]
- Spinal Muscular Atrophy Type I [MeSH concept]
- juvenile spinal muscular atrophy [MeSH concept]
- muscular atrophy, spinal, type II [MeSH concept]
Related record
- spinal muscular atrophies of childhood [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spinal Muscular Atrophy of Childhood [NCIt concept]
- childhood spinal muscular atrophy [DO Concept]
- spinal muscular atrophies of childhood [Disease (Nov.)]
Validated automatic mappings to BTNT
- Proximal spinal muscular atrophy type 1 [ORDO Disease]