Desmin bodies
Symptom Information:
Symptom ID: | HPO:0100300 | ||
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) Abnormality of muscle fibers(HPO:0004303) Muscle fiber inclusion bodies(HPO:0100299) Muscle fiber cytoplasmatic inclusion bodies(HPO:0100303) Desmin bodies(HPO:0100300) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Cardiomyopathy, familial restrictive 2 | (OMIM:609578) |