Difficulty running

Symptom Information:

Symptom ID: HPO:0009046
Synonyms:
Difficulty running [OMIM:Difficulty running]
Quality:
Cross references:
OMIM: "Difficulty running" [OMIM:Difficulty running]
Is a (Direct Parents):
HPO         Functional motor problems
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:
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)