Axial muscle weakness
Symptom Information:
Symptom ID: | HPO:0003327 | ||
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 physiology(HPO:0011804) Muscle weakness(HPO:0001324) Axial muscle weakness(HPO:0003327) MedDRA: |
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Database Frequency: | 10 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures | (Orphanet:363454) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Desmin-related myopathy with Mallory body-like inclusions | (Orphanet:84132) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
Rigid spine syndrome | (Orphanet:97244) |