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