Factor XII Deficiency, Variant 3 (Feline)

Category:

Haemolymphatic - Associated with the blood and lymph

Gene:

F12

Variant Detected:

c.1631G>C

Severity:

Low. This disease generally causes mild signs of disease, or can be quite easily treated/managed.

Mode of Inheritance:

Autosomal Recessive

Associated Breed(s):

Mixed Breed / Unknown Breed (Feline),