Type 1 muscle fiber predominance
Symptom Information:
Symptom ID: | HPO:0003803 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |