Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms. [ Orphanet : 326 ]
This is just here as a test because I lose it
Term information
database
cross reference
- MESH:D005166 (MONDO:equivalentTo)
- ICD10CM:D68.2 (Orphanet:326/ntbt)
- NCIT:C98938 (MONDO:equivalentTo)
- Orphanet:326 (OMIM:227400)
- GARD:0002237 (MONDO:equivalentTo)
- OMIM:227400 (Orphanet:326/e)
- DOID:2216 (MONDO:equivalentTo)
- UMLS:C0015499 (Orphanet:326/e)
- MedDRA:10048930 (Orphanet:326/e)
- SCTID:88776002 (MONDO:equivalentTo)
Subsets
gard_rare, ordo_disease
closeMatch
- http://identifiers.org/meddra/10048930
definition
- Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.
exactMatch
- http://www.orpha.net/ORDO/Orphanet_326
- http://purl.obolibrary.org/obo/DOID_2216
- http://identifiers.org/snomedct/88776002
- http://linkedlifedata.com/resource/umls/id/C0015499
- https://omim.org/entry/227400
- http://identifiers.org/mesh/D005166
- http://purl.obolibrary.org/obo/NCIT_C98938
has exact synonym
- hereditary factor V deficiency
- labile factor deficiency
- Owren disease
- Parahemophilia
- congenital factor V deficiency
- Proaccelerin deficiency
- deficiency, labile
- hereditary Factor V deficiency
- hereditary hypoproaccelerinaemia
has related synonym
- factor 5 deficiency
- factor V deficiency
- labile Factor deficiency
- Owren Parahemophilia
id
- MONDO:0009210
narrowMatch
- http://apps.who.int/classifications/icd10/browse/2010/en#/D68.2
seeAlso
- https://rarediseases.info.nih.gov/diseases/2237/factor-v-deficiency
Term relations
Equivalent to:
- factor V deficiency and has modifier some inherited