spinal muscular atrophy, distal, autosomal recessive, 3

Preferred Label : spinal muscular atrophy, distal, autosomal recessive, 3;

MeSH synonym : HMN III; HMN IV; HMN3; DHMN3; neuronopathy, distal hereditary motor, type III; neuronopathy, distal hereditary motor, type IV; neuropathy, distal hereditary motor, type IV; DHMN4; DSMA3; HMN4;

Details

Origin ID

C564626;

UMLS CUI

C1846823;

Currated CISMeF NLP mapping
- Autosomal recessive distal spinal muscular atrophy type 3 (disorder) [SNOMED CT concept]
- Distal spinal muscular atrophy type 3 [ORDO Disease]
- Neuronopathy, distal hereditary motor, autosomal recessive 3 [OMIM Phenotype]
- distal spinal muscular atrophy type 3 [DO Concept]
DO Cross reference
- distal spinal muscular atrophy type 3 [DO Concept]
MeSH term(s) associated for indexing
- muscular atrophy, spinal [MeSH Descriptor]
Record concept(s)
- spinal muscular atrophy, distal, autosomal recessive, 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive distal spinal muscular atrophy type 3 (disorder) [SNOMED CT concept]
- Distal spinal muscular atrophy type 3 [ORDO Disease]
- Neuronopathy, distal hereditary motor, autosomal recessive 3 [OMIM Phenotype]
- distal spinal muscular atrophy type 3 [DO Concept]

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