Burmese

The feline albino mutation is a rare mutation that produces a white coat with blue eyes, and is recessive to the sepia and Siamese mutations.

GM2 gangliosidosis is a degenerative, fatal neurological disease characterized by severe muscle tremors and loss of motor control.

Burmese hypokalemia is an inherited disorder found in Burmese cats that is characterized by skeletal muscle weakness that can cause affected cats to have trouble walking and holding their heads correctly.

Burmese head defect (BHD), or congenital frontonasal dysplasia, is an inherited defect found in Burmese cats that is characterized by improper development and subsequent malformation of the skull and facial features.