Late-onset distal muscle weakness
Symptom Information:
Symptom ID: | HPO:0003810 | ||
Synonyms: |
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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 physiology(HPO:0011804) Muscle weakness(HPO:0001324) Distal muscle weakness(HPO:0002460) Late-onset distal muscle weakness(HPO:0003810) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |