Muscle fiber splitting
Symptom Information:
Symptom ID: | HPO:0003555 | |||||
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) Muscle fiber splitting(HPO:0003555) MedDRA: |
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Database Frequency: | 11 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Alpha-crystallinopathy | (Orphanet:98910) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Muscle filaminopathy | (Orphanet:171445) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
VACUOLAR NEUROMYOPATHY | (OMIM:601846) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |