Orthopedics > OCOSH Classification > Systemic Disorders

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Systemic disorders that affect the musculoskeletal system. No equivalent MeSH term or unique ID Systemic disorders of connective tissue in diseases classified elsewhere [OCOSH Code: 56019007 M36 SD]

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Drug Reaction (5)
Drugs and medications used for orthopedic conditions and causing musculoskeletal problems
MeSH Search Term "Drug Therapy"[mesh] or "Drug Therapy/adverse effects"[mesh]
ICD-10 Code Y40-Y59 Drugs, medicaments and biological substances causing adverse effects in therapeutic use
SNOMED-CT Term Adverse reaction to drug (disorder) Concept ID: 62014003
Synonyms - Drug reaction
Adverse drug effect
Adverse drug reaction
Adverse reaction to drug
ADR - Adverse drug reaction
OCOSH Code: D004358 62014003 Y40-Y59 SD_D
Haemophilia (9)
Internet resources describing Orthopaedic complications of hemophilia. The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. Orthopaedic complications include acute hemarthrosis, bleeds into muscle and chronic hemophiliac arthropathy
MeSH Search Term "Hemophilia A"[mesh]
ICD-10 Code D66 Hereditary factor VIII deficiency
See also M36.2 Haemophilic arthropathy
SNOMED-CT Term Hemophilia (disorder) Concept ID: 90935002
Synonyms - Haemophilia
See also 80813006 Hemophilic arthropathy (disorder)
OCOSH Code: D006467 90935002 D66 M36.2 SD_H
Sarcoid (6)
Internet resources relating to orthopaedic manifestations of sarcoidosis
MeSH Search Term "Sarcoidosis"[mesh]
ICD-10 Code D86 Sarcoidosis
SNOMED-CT Term Sarcoidosis (disorder) Concept ID: 31541009
Synonyms - Boeck's sarcoid
Besnier-Boeck-Schaumann syndrome
Miliary lupoid of Boeck
Lupus pernio of Besnier
Benign lymphogranulomatosis of Schaumann
Darier-Roussy sarcoid
Boeck's sarcoidosis
OCOSH Code: D012507 31541009 D86 SD_SA
Sickle Cell Anemia (33)
Musculoskeletal aspect of Sickle Cell Disease, including osteomyelitis, septic arthritis, acute bone infraction and avascular necrosis. A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs.
MeSH Search Term "Anemia, Sickle Cell"[mesh]
ICD-10 Code D57 Sickle-cell disorders
SNOMED-CT Term Sickling disorder due to hemoglobin S (disorder) Concept ID: 417357006
Synonyms - Sickling disorder due to haemoglobin S
Sickle cell disease
Sickle cell syndrome
OCOSH Code: D000755 417357006 D57 SD_SCD


2011 Distinguishing fibromyalgia from rheumatoid arthritis and systemic lupus in clinical questionnaires

Location: http://arthritis-research.com/content/13/2/R58/abstract

Conclusions A combination of 2 questions ("tenderness to touch" and "difficulty sitting for 45 minutes") plus pain in the lower back, neck, hands and arms, may be useful in the construction of clinical questionnaires aimed at patients with musculoskeletal pain. This combination provided a correct diagnosis in 97% of subjects, with...

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Congenital and Metabolic Diseases

Location: http://www.thedoctorsdoctor.com/diseases/congenital_metabolic.htm

There is no single unifying trait for these disorders. Some have their genetic defect well characterized. Others are still waiting for the discovery of the gene or genes which are damaged. The diagnosis requires careful clinical laboratory evaluation and may require testing for enzymes that are...

View Details Visit Resource Review It Rate It Bookmark It Added: Wed Nov 29 2006