has material basis in germline mutation in disease arises from feature disease has basis in feature F7 Reduced factor VII activity factor VII deficiency congenital factor VII deficiency https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/factor_vii_deficiency DOID:2215 MONDO:0009211 NCIT:C131631 congenital proconvertin deficiency Orphanet:327 congenital factor VII deficiency Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor. UMLS:C0272320 OMIM:227500 hypoproconvertinemia MEDGEN:473015 MedDRA:10016079 factor 7 deficiency GARD:0002238 congenital vitamin K-dependent coagulation factors deficiency