Progressive proximal muscle weakness
Symptom Information:
Symptom ID: | HPO:0009073 | |||
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) Proximal muscle weakness(HPO:0003701) Progressive proximal muscle weakness(HPO:0009073) MedDRA: |
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Database Frequency: | 8 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE | (OMIM:300717) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT | (OMIM:300695) |
X-linked immunoneurologic disorder | (Orphanet:2571) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |
ZASP-related myofibrillar myopathy | (Orphanet:98912) |