Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor. [ Orphanet : 327 ]
This is just here as a test because I lose it
Term information
database
cross reference
- OMIM:227500 (Orphanet:327/e)
- GARD:0002238 (MONDO:equivalentTo)
- NCIT:C131631 (MONDO:equivalentTo)
- Orphanet:327 (OMIM:227500)
- DOID:2215 (MONDO:equivalentTo)
- UMLS:C1394919 (MONDO:equivalentTo)
- MedDRA:10016079 (Orphanet:327/e)
Subsets
ordo_disease
closeMatch
- http://identifiers.org/meddra/10016079
definition
- Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor.
exactMatch
- https://omim.org/entry/227500
- http://www.orpha.net/ORDO/Orphanet_327
- http://purl.obolibrary.org/obo/NCIT_C131631
- http://linkedlifedata.com/resource/umls/id/C1394919
- http://purl.obolibrary.org/obo/DOID_2215
has exact synonym
- hypoproconvertinemia
- congenital factor VII deficiency
- congenital proconvertin deficiency
has related synonym
- factor 7 deficiency
- factor VII deficiency
- F7 deficiency
id
- MONDO:0009211
term tracker item
- https://github.com/monarch-initiative/mondo/issues/4069