Categories: Haematopoietic system phene

Possible human homologues (MIM numbers): 227500 (trait) , 613878 (gene)

Links to relevant human diseases in MONDO:

• MONDO:0009211: congenital factor VII deficiency

Cross-species summary: Bleeding disorder due to deficiency of factor VII, a vitamin K–dependent glycoprotein. In humans also called Alexander's disease; proconvertin deficiency; prothrombin conversion accelerator deficiency; hypoproconvertinaemia.

Species in which this phene is found:
dog (Canis lupus familiaris)
Asiatic elephant (Elephas maximus)