Muscle stiffness
Symptom Information:
Symptom ID: | HPO:0003552 | ||
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 stiffness(HPO:0003552) MedDRA: |
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Database Frequency: | 23 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acetazolamide-responsive myotonia | (Orphanet:99736) |
Autosomal recessive axonal neuropathy with neuromyotonia | (Orphanet:324442) |
Carnitine palmitoyl transferase II deficiency | (Orphanet:157) |
Carnitine palmitoyl transferase II deficiency, myopathic form | (Orphanet:228302) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency | (Orphanet:284426) |
Glycogen storage disease due to lactate dehydrogenase deficiency | (Orphanet:2364) |
HYPEREKPLEXIA 3 | (OMIM:614618) |
MYOTONIA CONGENITA, AUTOSOMAL DOMINANT | (OMIM:160800) |
MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE | (OMIM:255700) |
MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS | (OMIM:160990) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |
Myotonia fluctuans | (Orphanet:99734) |
Myotonia permanens | (Orphanet:99735) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
Paramyotonia congenita of Von Eulenburg | (Orphanet:684) |
Potassium-aggravated myotonia | (Orphanet:612) |
Pyruvate dehydrogenase E2 deficiency | (Orphanet:79244) |
SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE | (OMIM:615625) |
TRAPS syndrome | (Orphanet:32960) |
Thomsen and Becker disease | (Orphanet:614) |
Tubular aggregate myopathy | (Orphanet:2593) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |