Hereditary factor XI deficiency

Preferred Label : Hereditary factor XI deficiency;

Inclusion CIM-10 : Plasma thromboplastin antecedent [PTA] deficiency; Hemophilia C; Rosenthal's disease;

Diag associé à un acte (%) : 83.3;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D681;

UMLS CUI

C0015523;

Automatic exact mappings (from CISMeF team)
- factor XI deficiency [DO Concept]
Currated CISMeF NLP mapping
- Congenital factor XI deficiency [ORDO Disease]
- Congenital factor XI deficiency [ICD-9 code]
- Factor XI deficiency [OMIM Phenotype]
- Factor XI deficiency [MedDRA Preferred Term]
- Haemophilia C [ICD-11 Category]
- Haemophilia C (Factor XI) [MedDRA LLT]
- Hemophilia C (Factor XI) [MedDRA LLT]
- Hereditary Factor XI Deficiency [NCIt concept]
- Hereditary factor XI deficiency [ICD-10 Sub-category (who)]
- Hereditary factor XI deficiency disease (disorder) [SNOMED CT concept]
- blood clotting factor xi deficiency [Disease (Nov.)]
- factor XI deficiency [MeSH concept]
- factor xi deficiency [MeSH Descriptor]
- hereditary factor xi deficiency disease [SNOMED Notion]
DO Cross reference
- factor XI deficiency [DO Concept]
Orphanet concepts
- Congenital factor XI deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital factor XI deficiency [MedDRA LLT]
- Congenital factor XI deficiency [ICD-9 code]
- Congenital factor XI deficiency [ORDO Disease]
- Factor XI deficiency [MedDRA Preferred Term]
- Factor XI deficiency [OMIM Phenotype]
- Haemophilia C (Factor XI) [MedDRA LLT]
- Hemophilia C (Factor XI) [MedDRA LLT]
- Hereditary Factor XI Deficiency [NCIt concept]
- Hereditary factor XI deficiency disease (disorder) [SNOMED CT concept]
- Reduced factor XI activity [HPO term]
- blood clotting factor xi deficiency [Disease (Nov.)]
- factor XI deficiency [MeSH concept]
- factor XI deficiency [DO Concept]
- factor xi deficiency [MeSH Descriptor]
- hereditary factor xi deficiency disease [SNOMED Notion]

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