Abnormality of muscle fibers

Symptom Information:

Symptom ID: HPO:0004303
Synonyms:
Abnormal skeletal muscle fiber morphology [HPO:0004303]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Reduced muscle carnitine level
HPO         Abnormality of muscle morphology
HPO         Central core regions in muscle fibers
HPO         Abnormal muscle fiber protein expression
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)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Greig cephalopolysyndactyly syndrome (Orphanet:380)
MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE (OMIM:159100)