scapuloperoneal form of spinal muscular atrophy

Preferred Label : scapuloperoneal form of spinal muscular atrophy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0335732;

UMLS CUI

C0751335;

Automatic exact mappings (from CISMeF team)
- Other inherited spinal muscular atrophy [ICD-10 Sub-category (who)]
- Scapuloperoneal form of spinal muscular atrophy [ICD-11 More detail]
Currated CISMeF NLP mapping
- Neurogenic scapuloperoneal syndrome, Kaeser type [ORDO Disease]
- Scapuloperoneal spinal muscular atrophy [ORDO Disease]
- Scapuloperoneal spinal muscular atrophy [OMIM Phenotype]
- Scapuloperoneal spinal muscular atrophy (disorder) [SNOMED CT concept]
- Scapuloperoneal syndrome, neurogenic, kaeser type [OMIM Phenotype]
- Spinal muscular atrophy, scapuloperoneal [OMIM Phenotype]
- scapuloperoneal spinal muscular atrophy [DO Concept]
- scapuloperoneal spinal muscular atrophy [Disease (Nov.)]
Related record
- muscular atrophy, spinal [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Scapuloperoneal spinal muscular atrophy [OMIM Phenotype]
- Scapuloperoneal spinal muscular atrophy [ORDO Disease]
- Scapuloperoneal spinal muscular atrophy (disorder) [SNOMED CT concept]
- Spinal muscular atrophy, scapuloperoneal [OMIM Phenotype]
- scapuloperoneal spinal muscular atrophy [Disease (Nov.)]
- scapuloperoneal spinal muscular atrophy [DO Concept]