Increased variability in muscle fiber diameter
Symptom Information:
Symptom ID: | HPO:0003557 | |||||||||
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) Abnormality of skeletal muscle fiber size(HPO:0012084) Increased variability in muscle fiber diameter(HPO:0003557) MedDRA: |
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Database Frequency: | 24 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Autosomal dominant optic atrophy and congenital deafness | (Orphanet:3212) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2H | (Orphanet:1878) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy with integrin alpha-7 deficiency | (Orphanet:34520) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
DPM3-CDG | (Orphanet:263494) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
Proximal myotonic myopathy | (Orphanet:606) |
Reducing body myopathy | (Orphanet:97239) |
Rigid spine syndrome | (Orphanet:97244) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Tubular aggregate myopathy | (Orphanet:2593) |