Nemaline bodies
Symptom Information:
Symptom ID: | HPO:0003798 | |||
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) Nemaline bodies(HPO:0003798) MedDRA: |
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Database Frequency: | 12 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
Cap myopathy | (Orphanet:171881) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Moderate multiminicore disease with hand involvement | (Orphanet:178145) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
NEMALINE MYOPATHY 4 | (OMIM:609285) |
NEMALINE MYOPATHY 5 | (OMIM:605355) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
NEMALINE MYOPATHY 7 | (OMIM:610687) |
NEMALINE MYOPATHY 8 | (OMIM:615348) |
Nemaline myopathy | (Orphanet:607) |