Primary thrombophilia

Preferred Label : Primary thrombophilia;

Inclusion CIM-10 : Primary hypercoagulable states;

ICD-10 exclusion note : secondary activated protein C resistance (D68.69); antiphospholipid syndrome (D68.61); lupus anticoagulant (D68.62); systemic lupus erythematosus [SLE] inhibitor finding without diagnosis (R76.0); thrombotic thrombocytopenic purpura (M31.1); secondary antiphospholipid antibody syndrome (D68.69); secondary lupus anticoagulant with hypercoagulable state (D68.69); systemic lupus erythematosus [SLE] inhibitor with hemorrhagic disorder (D68.312); secondary systemic lupus erythematosus [SLE] inhibitor with hypercoagulable state (D68.69);

Source : OMS;

Date de début : 01/01/2009;

Détails

Origin ID

D685;

UMLS CUI

C2584620;

Automatic exact mappings (from CISMeF team)
- Hereditary thrombophilia (disorder) [SNOMED CT concept]
- Protein C Deficiency Disease [NCIt concept]
- Protein S Deficiency Disease [NCIt concept]
- protein C deficiency [MeSH concept]
- protein S deficiency [MeSH concept]
- protein c deficiency [MeSH Descriptor]
- protein s deficiency [MeSH Descriptor]
Orphanet concepts
- Hereditary thrombophilia due to congenital antithrombin deficiency [ORDO Disease]
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency [ORDO Disease]
- Non rare thrombophilia [ORDO Disease]
- Rare hereditary thrombophilia [ORDO Disease]
- Severe hereditary thrombophilia due to congenital protein S deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary thrombophilia [ICD-11 Subcategory]
- Hereditary thrombophilia (disorder) [SNOMED CT concept]
- Rare hereditary thrombophilia [ORDO Disease]
- Thrombophilia, hereditary [MeSH concept]
- thrombophilia, hereditary [MeSH Supplementary Concept]
Validated automatic mappings to BTNT
- Hereditary thrombophilia [ICD-11 Subcategory]

Position du mot-clé dans l'(les) arborescence(s) :

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