Type 2 muscle fiber predominance

Symptom Information:

Symptom ID: HPO:0010602
Synonyms:
Type II muscle fiber predominance [HPO:0010602]
Type 2 muscle fiber predominance [OMIM:Type 2 muscle fiber predominance]
Quality:
Cross references:
OMIM: "Type 2 muscle fiber predominance" [OMIM:Type 2 muscle fiber predominance]
Is a (Direct Parents):
HPO         Abnormality of muscle fibers
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Abnormality of muscle fibers(HPO:0004303)
                Type 2 muscle fiber predominance(HPO:0010602)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures (Orphanet:209341)