Difficulty running
Symptom Information:
Symptom ID: | HPO:0009046 | ||
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) Functional motor problems(HPO:0004302) Difficulty running(HPO:0009046) MedDRA: |
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Database Frequency: | 17 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures | (Orphanet:363454) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | (Orphanet:209341) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
MIYOSHI MUSCULAR DYSTROPHY 3 | (OMIM:613319) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID | (OMIM:615575) |
Neutral lipid storage myopathy | (Orphanet:98908) |
PEROXISOME BIOGENESIS DISORDER 5B | (OMIM:614867) |
Tubular aggregate myopathy | (Orphanet:2593) |
X-linked myopathy with excessive autophagy | (Orphanet:25980) |