Increased variability in muscle fiber diameter

Symptom Information:

Symptom ID: HPO:0003557
Synonyms:
Increased fiber size variation [HPO:0003557]
Increased variability in muscle fiber size [HPO:0003557]
Increased variation in fiber size [HPO:0003557]
Increased variation in muscle fiber size [HPO:0003557]
Variation in muscle fiber size [HPO:0003557]
Increased fiber size variation [OMIM:Increased fiber size variation]
Increased variation in fiber size [OMIM:Increased variation in fiber size]
Increased variation in muscle fiber size [OMIM:Increased variation in muscle fiber size]
Variation in muscle fiber size [OMIM:Variation in muscle fiber size]
Quality:
Cross references:
OMIM: "Increased fiber size variation" [OMIM:Increased fiber size variation]
OMIM: "Increased variation in fiber size" [OMIM:Increased variation in fiber size]
OMIM: "Increased variation in muscle fiber size" [OMIM:Increased variation in muscle fiber size]
OMIM: "Variation in muscle fiber size" [OMIM:Variation in muscle fiber size]
Is a (Direct Parents):
HPO         Abnormality of skeletal muscle fiber size
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:
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)