Muscle fiber necrosis

Symptom Information:

Symptom ID: HPO:0003713
Muscle fiber necrosis [OMIM:Muscle fiber necrosis]
Cross references:
OMIM: "Muscle fiber necrosis" [OMIM:Muscle fiber necrosis]
Is a (Direct Parents):
HPO         Abnormality of muscle fibers
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Abnormality of muscle fibers(HPO:0004303)
                Muscle fiber necrosis(HPO:0003713)
Database Frequency: 8 / 7739

All diseases associated with this symptom:

Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
DPM3-CDG (Orphanet:263494)
Duchenne muscular dystrophy (Orphanet:98896)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)