factor V deficiency

Preferred Label : factor V deficiency;

CISMeF synonym : Diseases, Owren; Diseases, Owren's; Owren Diseases; Owren's Diseases;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0008143;

UMLS CUI

C0015499;

Automatic exact mappings (from CISMeF team)
- Hereditary deficiency of other clotting factors [ICD-10 Sub-category (who)]
- Hereditary factor V deficiency [ICD-11 More detail]
- factor V deficiency [DO Concept]
Currated CISMeF NLP mapping
- Congenital factor V deficiency [ORDO Disease]
- Factor V Deficiency [NCIt concept]
- Factor V deficiency [MedDRA Preferred Term]
- Factor V deficiency [OMIM Phenotype]
- Factor V deficiency (disorder) [SNOMED CT concept]
- Hereditary Factor V Deficiency [NCIt concept]
- Hereditary factor V deficiency disease (disorder) [SNOMED CT concept]
- Reduced coagulation factor V activity [HPO term]
- blood clotting factor v deficiency [Disease (Nov.)]
- factor v deficiency [Blood Transfusion thesaurus concept]
- factor v deficiency, nos [SNOMED Notion]
- hereditary factor v deficiency disease [SNOMED Notion]
Related record
- factor v deficiency [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital factor V deficiency [ORDO Disease]
- Factor V deficiency [OMIM Phenotype]
- Hereditary Factor V Deficiency [NCIt concept]
- Hereditary factor V deficiency disease (disorder) [SNOMED CT concept]
- Reduced coagulation factor V activity [HPO term]
- factor V deficiency [DO Concept]
- factor v deficiency, nos [SNOMED Notion]
- hereditary factor v deficiency disease [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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