Type 1 muscle fiber predominance

Symptom Information:

Symptom ID: HPO:0003803
Synonyms:
Type I muscle fiber predominance [HPO:0003803]
Type 1 muscle fiber predominance [OMIM:Type 1 muscle fiber predominance]
Quality:
Cross references:
OMIM: "Type 1 muscle fiber predominance" [OMIM:Type 1 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 1 muscle fiber predominance(HPO:0003803)
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Central core disease (Orphanet:597)
Combined oxidative phosphorylation defect type 13 (Orphanet:319514)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Congenital myopathy with excess of thin filaments (Orphanet:98904)
Hyaline body myopathy (Orphanet:53698)
Laing distal myopathy (Orphanet:59135)
MYOPATHY, MYOSIN STORAGE (OMIM:608358)
Moderate multiminicore disease with hand involvement (Orphanet:178145)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEMALINE MYOPATHY 5 (OMIM:605355)
Nemaline myopathy (Orphanet:607)