Bernardoodle - Full Breed Profile

Full Breed Profile includes:

Diseases:

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Autosomal Hereditary Recessive Nephropathy

Congenital Macrothrombocytopenia

Congenital Methemoglobinemia (Poodle and Pomeranian Type)

Curly Coat Dry Eye Syndrome (Cavalier Type)

Degenerative Myelopathy

Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

Episodic Falling Syndrome (Cavalier Type)

Exercise Induced Collapse (Retriever Type)

Osteochondrodysplasia (Min Poodle Type)

Phosphofructokinase Deficiency (Spaniel Type)

Polyneuropathy GJA9 (Leonberger/St Bernard Type)

Progressive Rod Cone Degeneration (prcd) - PRA

von Willebrand's Disease Type I

Traits:

E Locus - (Cream/Red/Yellow)

I Pheomelanin Locus Colour Intensity

Brown Deletion = Bd

Brown Stop Codon = Bs

Brown Insertion = Bc

Brown TYRP1 [Lancashire Heeler Type] = Bl

D (Dilute) Locus

K Locus (Dominant Black)

A Locus (Agouti)

Pied (BOTH SINE and REPEAT VARIANTS)

M Locus (Merle/Dapple)

Black Hair Follicular Dysplasia

Shedding (MC5R)

Coat Composition CFA28 Gene (Double/Single Coat)

Curly Coat/Hair Curl (KRT71 R151W)