spinal muscular atrophy, Late-Onset, finkel type

Preferred Label : spinal muscular atrophy, Late-Onset, finkel type;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566973;

UMLS CUI

C1854058;

Currated CISMeF NLP mapping
- Autosomal dominant adult-onset proximal spinal muscular atrophy [ORDO Disease]
- Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder) [SNOMED CT concept]
- Autosomal dominant proximal spinal muscular atrophy, adult-onset [ICD-11 More detail]
- Spinal muscular atrophy, late-onset, finkel type [OMIM Phenotype]
- autosomal dominant adult-onset proximal spinal muscular atrophy [DO Concept]
Related record
- spinal muscular atrophy, Late-Onset, finkel type [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant adult-onset proximal spinal muscular atrophy [ORDO Disease]
- Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder) [SNOMED CT concept]
- Spinal muscular atrophy, late-onset, finkel type [OMIM Phenotype]