Myofibrillar myopathy

Symptom Information:

Symptom ID: HPO:0003715
Synonyms:
Myofibrillar changes [HPO:0003715]
Myofibrillar myopathy [OMIM:Myofibrillar myopathy]
Quality:
Cross references:
OMIM: "Myofibrillar myopathy" [OMIM:Myofibrillar myopathy]
Is a (Direct Parents):
HPO         Myopathy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Myopathy(HPO:0003198)
                Myofibrillar myopathy(HPO:0003715)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Cardiomyopathy, familial restrictive, 1 (OMIM:115210)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Muscle filaminopathy (Orphanet:171445)
Muscular dystrophy, Selcen type (Orphanet:199340)
Myotilin-related myofibrillar myopathy without spheroid body (Orphanet:98911)
NEMALINE MYOPATHY 8 (OMIM:615348)
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT (OMIM:300695)
ZASP-related myofibrillar myopathy (Orphanet:98912)