hemophilia - CISMeF

Preferred Label : hemophilia;

MedlinePlus synonym : blood coagulation disorders; christmas disease; factor viii deficiency; factor ix deficiency;

Details

Origin ID

T3115;

UMLS CUI

C0684275;

Automatic exact mappings (from CISMeF team)
- Abnormality of coagulation [HPO term]
- Blood coagulation disorder (disorder) [SNOMED CT concept]
- Factor IX deficiency (disorder) [SNOMED CT concept]
- Haemophilia C [ICD-11 Category]
- Hemi-neglect (finding) [SNOMED CT concept]
- Hemophilia [ACR pathology]
- Hemophilia [LOINC component]
- Hemophilia [ACR pathology]
- Hemophilia [ACR pathology]
- Hemophilia [ACR pathology]
- Hemophilia - specialty (qualifier value) [SNOMED CT concept]
- Hemophilia A without inhibitors [MedDRA LLT]
- blood coagulation disorder [Blood Transfusion thesaurus concept]
- blood coagulation disorders [MeSH Descriptor]
- blood coagulation disorders [MeSH concept]
- coagulation factor IX [ORDO Gene]
- coagulation factor IX [HGNC gene]
- coagulation factor VIII [ORDO Gene]
- coagulation factor VIII [HGNC gene]
- factor VIII deficiency [DO Concept]
- factor xi deficiency [MeSH Descriptor]
- purpura - coagulation defect [ICPC-2 Rubric]
CISMeF manual mappings
- Hemophilia A [ORDO Disease]
Currated CISMeF NLP mapping
- Factor IX deficiency [MedDRA Preferred Term]
- Factor VIII deficiency [MedDRA Preferred Term]
- Factor VIII deficiency [OMIM Phenotype]
- Factor VIII deficiency (disorder) [SNOMED CT concept]
- Haemophilia [MedDRA Preferred Term]
- Haemophilia [HPMULTI term]
- Haemophilia A [ICD-11 Subcategory]
- Haemophilia A [MedDRA LLT]
- Haemophilia NOS [MedDRA LLT]
- Hemophilia [PASCAL descriptor]
- Hemophilia [NCIt concept]
- Hemophilia [ORDO Disease]
- Hemophilia [MedDRA LLT]
- Hemophilia (disorder) [SNOMED CT concept]
- Hemophilia A [MedDRA LLT]
- Hemophilia A [PASCAL descriptor]
- Hemophilia A [NCIt concept]
- Hemophilia A (Factor VIII) [MedDRA LLT]
- Hemophilia B [PASCAL descriptor]
- Hemophilia B [NCIt concept]
- Hemophilia B [ORDO Disease]
- Hemophilia a [OMIM Phenotype]
- Hemophilia b [OMIM Phenotype]
- Hereditary factor IX deficiency [ICD-10 category]
- Hereditary factor IX deficiency disease (disorder) [SNOMED CT concept]
- Hereditary factor VIII deficiency [ICD-10 category]
- Hereditary factor VIII deficiency [ICD-10 category (who)]
- Hereditary factor VIII deficiency disease (disorder) [SNOMED CT concept]
- Reduced factor VIII activity [HPO term]
- factor VIII deficiency [MeSH concept]
- haemophilia [Blood Transfusion thesaurus concept]
- hemophilia [Disease (Nov.)]
- hemophilia A [Disease (Nov.)]
- hemophilia A [MeSH Descriptor]
- hemophilia A [MeSH concept]
- hemophilia A [Blood Transfusion thesaurus concept]
- hemophilia B [DO Concept]
- hemophilia B [MeSH concept]
- hemophilia B [MeSH Descriptor]
- hemophilia B [Blood Transfusion thesaurus concept]
- hemophilia a, nos [SNOMED Notion]
- hemophilia b, nos [SNOMED Notion]
- hemophilia, nos [SNOMED Notion]
MeSH descriptor(s)
- blood coagulation disorders [MeSH Descriptor]
- hemophilia A [MeSH Descriptor]
See also
- bleeding disorders [MedlinePlus Topic]
- blood disorders [MedlinePlus Topic]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Haemophilia B [ICD-11 Subcategory]
- Hereditary factor IX deficiency [ICD-11 Category]

Keyword's position in hierarchy(ies) :

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