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26601000087101: Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2020. Module: Canada Health Infoway English module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
133241000087117 Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept) en Fully specified name Active Entire term case insensitive (core metadata concept) Canada Health Infoway English module (core metadata concept)
133251000087119 Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Canada Health Infoway English module (core metadata concept)
133261000087116 Health concern code subset commonly used reference set en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Canada Health Infoway English module (core metadata concept)
133311000087113 Represents the most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider en Definition Active Entire term case sensitive (core metadata concept) Canada Health Infoway English module (core metadata concept)


4219 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept) est un(e) (attribut) ensemble de référence simple canadien true Inferred relationship Some

Members
Granulomatous hepatitis
Granulosa cell tumour of ovary
Graphomotor aphasia
maladie de Graves
Grey platelet syndrome
bursite trochantérienne
syndrome de céphalopolysyndactylie de Greig (trouble)
grincement de dents
Gross motor impairment
Growing pains
gynécomastie (trouble)
Hemolysis-elevated liver enzymes-low platelet count syndrome (disorder)
Habitual eating of own hair
Hairy cell leukemia (clinical)
hallucinations (constatation)
Hallux valgus AND bunion
Hammer toe
Enteroviral vesicular stomatitis with exanthem
Health maintenance alteration
perte auditive (trouble)
Hearing problem
Heart block
Heart failure
Heart murmur
Heart valve disorder
brûlures d'estomac (constatation)
Heat exhaustion
Heavy chain disease
Heavy metal food poisoning
Hecht syndrome
infection du tractus gastro-intestinal par Helicobacter pylori
Hemangioma of liver
Hemangiopericytoma
Hemarthrosis
Hematemesis
Hematotympanum
Hemianesthesia
Hemianopia
Hemichorea
Hemifacial spasm
Hemihypertrophy of muscle
hémimégalencéphalie
Hemiparesis
hémiplégie
paralysie cérébrale hémiplégique
migraine hémiplégique
Hemispheric retinal vein occlusion
Haemoglobin Bart's hydrops syndrome
Hemoglobin H constant spring thalassemia (disorder)
Hemoglobin Lepore trait
Hemoglobin SS disease with crisis (disorder)
Hemoglobinopathy
Hemolysis
Hemolytic anemia
Hemolytic uremic syndrome
Haemophagocytic lymphohistiocytosis
Hemophilia
Hemophilia carrier (finding)
Hemoptysis
Hemorrhage of kidney
infarctus cérébral hémorragique
Hemorrhagic complication of pregnancy
Hemorrhagic shock
hémorroïdes (trouble)
Haemosiderosis
Heparin-induced thrombocytopenia
Heparin-induced thrombocytopenia with thrombosis
Hepatic artery thrombosis
encéphalopathie hépatique
insuffisance hépatique (trouble)
Hepatic infarction
porphyrie hépatique (trouble)
Hepatic sclerosis
porteur de l'hépatite B
porteur de l'hépatite C
Hepatopulmonary syndrome (disorder)
hépatosplénomégalie
Hereditary C1 esterase inhibitor deficiency - deficient factor
acrodermatite entéropathique héréditaire (trouble)
Hereditary angioedema with normal C1 esterase inhibitor activity
Hereditary coagulation factor deficiency
Hereditary coproporphyria
Hereditary dysfibrinogenemia (disorder)
Hereditary factor IX deficiency disease (disorder)
Hereditary liability to pressure palsies
lymphœdème héréditaire
Hereditary lymphedema type I (disorder)
Hereditary lymphedema type II (disorder)
Hereditary macular dystrophy
Hereditary nephritis (disorder)
Hereditary pancreatitis
Hereditary pyropoikilocytosis
Hereditary sensory and autonomic neuropathy type II (disorder)
paraplégie spastique héréditaire (trouble)
sphérocytose héréditaire
Hereditary stomatocytosis
Hereditary von Willebrand disease type 2M
Hermansky-Pudlak syndrome
hernie de la cavité abdominale
Herpes labialis
infection à herpès simplex

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