Rimmed vacuoles
Symptom Information:
Symptom ID: | HPO:0003805 | |||||
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) Rimmed vacuoles(HPO:0003805) MedDRA: |
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Database Frequency: | 22 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 20 | (OMIM:615426) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Autosomal dominant limb-girdle muscular dystrophy type 1G | (Orphanet:55596) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
DPM3-CDG | (Orphanet:263494) |
Distal myopathy with early respiratory muscle involvement | (Orphanet:34521) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Distal myopathy, Nonaka type | (Orphanet:602) |
Distal myopathy, Welander type | (Orphanet:603) |
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE | (OMIM:600737) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 | (OMIM:615424) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
Inclusion body myositis | (Orphanet:611) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
NONAKA MYOPATHY | (OMIM:605820) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
Tibial muscular dystrophy | (Orphanet:609) |
VACUOLAR NEUROMYOPATHY | (OMIM:601846) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |