Other specified hemorrhagic conditions

Preferred Label : Other specified hemorrhagic conditions;

Inclusion CIM-10 : Vascular pseudohemophilia; Capillary fragility (hereditary);

Diag associé à un acte (%) : 74.1;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D698;

UMLS CUI

C0029804;

Automatic exact mappings (from CISMeF team)
- Hereditary vascular purpura [ICD-11 Subcategory]
- von Willebrand's disease [DO Concept]
- von willebrand diseases [MeSH Descriptor]
DO Cross reference
- platelet-type bleeding disorder 11 [DO Concept]
- platelet-type bleeding disorder 3 [DO Concept]
- platelet-type bleeding disorder 8 [DO Concept]
- platelet-type bleeding disorder 9 [DO Concept]
Excluded by
- Von Willebrand's disease [ICD-10 Sub-category]
Orphanet concepts
- Bleeding diathesis due to a collagen receptor defect [ORDO Disease]
- Bleeding diathesis due to glycoprotein VI deficiency [ORDO Disease]
- Bleeding diathesis due to integrin alpha2-beta1 deficiency [ORDO Disease]
- Bleeding diathesis due to thromboxane synthesis deficiency [ORDO Disease]
- Bleeding disorder due to P2Y12 defect [ORDO Disease]
- Pseudo-von Willebrand disease [ORDO Disease]
- Rare hemorrhagic disorder due to a qualitative platelet defect [ORDO Disease]
- Scott syndrome [ORDO Disease]
- Stormorken-Sjaastad-Langslet syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Other Specified Hemorrhagic Conditions [NCIt concept]
- Other specified hemorrhagic conditions [ICD-9 code]
Validated automatic mappings to BTNT
- Hereditary vascular fragility (disorder) [SNOMED CT concept]
- platelet-type bleeding disorder 11 [DO Concept]
- platelet-type bleeding disorder 8 [DO Concept]
- platelet-type bleeding disorder 9 [DO Concept]

Keyword's position in hierarchy(ies) :

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