Exciting News from Orivet: 25 New Tests Added to Our Comprehensive Breed Profiles!

This test identifies genetic factors associated with congenital deafness in Australian Cattle and Stumpy Cattle Dog breeds, allowing for early intervention and management.

Tailored for Italian Greyhounds, this test screens for genetic mutations linked to muscular dystrophy, aiding in early diagnosis and potential treatment options.

This test targets Staffordshire Terriers, detecting genetic variants associated with muscular dystrophy to facilitate proactive health management.

This test detects genetic markers associated with night blindness, enabling breeders to make informed breeding decisions and prevent the spread of this condition.

Targeting Eurasier breeds, this test identifies genetic variants linked to Dandy Walker Like Malformation, providing breeders with valuable information for breeding programs and potential health management strategies.

This test assesses genetic predispositions to early-onset degenerative myelopathy, empowering breeders with knowledge to prevent and manage this debilitating condition.

This test detects genetic markers associated with ECLE in Pointers and Vizslas, offering breeders insights to mitigate risks and ensure the health of future generations.

Tailored for Jack Russell Terriers, this test identifies genetic variants associated with gastrointestinal polyposis, aiding breeders in making informed breeding decisions and minimising the prevalence of this condition.

This test screens for genetic mutations linked to globoid cell leukodystrophy in Irish Setters, enabling breeders to avoid breeding affected individuals and reduce the incidence of this disorder.

These tests screen for genetic mutations linked to haemophilia A and B in Rhodesian Ridgebacks, allowing breeders to avoid breeding affected individuals and reduce the incidence of these bleeding disorders.

This test detects genetic variants associated with intestinal cobalamin malabsorption in Giant Schnauzers, providing breeders with valuable information to prevent the transmission of this metabolic disorder.

Tailored exclusively for Staffordshire Bull Terriers, this test pinpoints variant 2 of L-2-hydroxyglutaric aciduria, providing breeders with invaluable insights to mitigate the transmission of this metabolic disorder within the breed.

This test screens for genetic mutations associated with L-2-hydroxyglutaric aciduria in Yorkshire Terriers, enabling breeders to avoid breeding affected individuals and reduce the incidence of this disorder.

Tailored for Shetland Sheepdogs, this test identifies genetic markers associated with PED, offering breeders insights to minimise the risk of this condition in their breeding programs.

These tests detect genetic mutations linked to early-onset progressive retinal atrophy in Tibetan Terriers and Spaniels, enabling breeders to make informed decisions to preserve vision in future generations.

These tests screen for genetic variants associated with severe combined immunodeficiency disease in various terrier breeds, Basset Hounds, and Corgis, empowering breeders with knowledge to prevent the transmission of this immunodeficiency disorder.

This test identifies genetic markers associated with startle disease, providing breeders with insights to minimise the risk of this neurological condition in their breeding programs.

This test explores the behavioral tendencies specific to Belgian Shepherds, providing breeders with valuable insights into temperament and personality traits.

Uncover the genetic basis of roan coat patterns and ticking in various breeds, shedding light on the distinctive markings that make each dog unique.

Explore the genetic variants responsible for the ancient red coat colour in Spitz and Scent Hound breeds, adding depth to breed standards and identification.

Dive into the genetic underpinnings of sable coat colouration in Cocker Spaniels and other breeds, enhancing understanding of coat genetics and breeding practices.