Myofibrillar myopathy
Symptom Information:
Symptom ID: | HPO:0003715 | ||
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) Myopathy(HPO:0003198) Myofibrillar myopathy(HPO:0003715) MedDRA: |
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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) |