Muscle stiffness

Symptom Information:

Symptom ID: HPO:0003552
Synonyms:
Muscle stiffness [OMIM:Muscle stiffness]
Muscle stiffness (in older patients) [OMIM:Muscle stiffness (in older patients)]
Quality:
Cross references:
OMIM: "Muscle stiffness" [OMIM:Muscle stiffness]
OMIM: "Muscle stiffness (in older patients)" [OMIM:Muscle stiffness (in older patients)]
Is a (Direct Parents):
HPO         Abnormality of muscle physiology
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:
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)