Metabolic Diseases genetic tests help identify inherited skin disorders in dogs, cats and horses using DNA analysis.
Metabolic diseases in animals are disorders that disrupt normal biochemical processes, often due to inherited genetic variants. These conditions can affect energy production, nutrient utilization, and waste elimination. Understanding these diseases is crucial for breeders and veterinarians, as DNA testing can identify at-risk individuals, guiding screening decisions and management strategies. Species-specific testing helps ensure the health and well-being of dogs, cats, and horses.
Looking for a DNA test related to metabolic diseases?
Browse animal DNA testsThis page currently lists 56 genetic tests related to metabolic diseases, including 38 for Dog, 18 for Cat.
Metabolic Diseases genetic tests are DNA-based laboratory analyses used to detect inherited variants associated with metabolic diseases. These tests can support veterinary screening, diagnostic interpretation, breeding decisions and long-term health management across different animal species.
This page lists 56 genetic tests related to metabolic diseases. The largest group is Dog with 38 tests, alongside additional screening options across other species.
This index lists the main genetic tests related to metabolic diseases currently available on this page, together with their species, genetic feature and variation type.
Each entry links to a detailed test page covering a specific inherited condition, biological pathway or clinically relevant genetic marker.
The table below shows the first 40 genetic tests for easier browsing. Use the button to expand the complete index.
The complete list of genetic tests continues below, organized by species. These sections help group screening options across dog, cat, horse and other represented animal populations.
These highlighted DNA tests provide a quick overview of commonly screened inherited variants related to metabolic diseases.
L-2-Hydroxyglutaric Aciduria (L2HGA) is a genetic disorder affecting Staffordshire Bull Terriers, caused by a mutation in the L2HGDH gene. This condition leads to the accumulation of L-2-hydroxyglutaric acid in the…
Associated with one or more specific breeds in the represented species.
Relevant across the breeds and not limited to a single breed.
Linked to a species without a clear breed-specific association.
In dogs, metabolic diseases can include conditions like portosystemic shunt and certain inherited enzyme deficiencies. DNA testing helps identify at-risk breeds.
Alpha-Mannosidosis (AMD) is a rare genetic disorder in dogs caused by a deficiency of the enzyme alpha-mannosidase. This enzyme deficiency leads to the accumulation of complex sugars in cells, causing…
Canine Malignant Hyperthermia (MH) is a rare genetic disorder triggered by certain anesthetic agents in dogs. It leads to a severe and uncontrolled increase in body temperature, muscle rigidity, and…
Copper Storage Disease (CSD) is a hereditary condition in Labrador Retrievers caused by a genetic mutation that affects copper metabolism. This disorder leads to the accumulation of copper in the…
Copper Toxicosis Variant 2 is a genetic condition in dogs that affects the liver's ability to process copper effectively. This can lead to dangerous copper accumulation, causing liver damage and…
A DNA test for Gallbladder Mucoceles (GM) in dogs helps identify genetic mutations linked to this condition. GM causes abnormal bile accumulation, leading to gallbladder dysfunction and potential health risks.…
Glycogen Storage Disease Ia in Maltese dogs (GSDIa-M) is a genetic disorder that affects the metabolism of glycogen, leading to its accumulation in the liver and muscles. This condition is…
Glycogen Storage Disease II (GSDII) in Lapphunds is a genetic disorder affecting the breakdown of glycogen in muscle cells. This condition leads to muscle weakness, respiratory difficulties, and reduced mobility…
Glycogen Storage Disease IIIa (GSDIIIa) is a genetic disorder in dogs that affects their ability to break down glycogen, leading to the accumulation of this complex carbohydrate in tissues. This…
Glycogen Storage Disease VII (GSDVII) is a genetic disorder in dogs caused by a deficiency in the enzyme muscle phosphofructokinase. This condition leads to the accumulation of glycogen in muscle…
Glycogen Storage Disease VII (GSDVII) is a hereditary condition affecting the Deutscher Wachtelhund, a breed known for its hunting prowess. This genetic disorder impairs the dog's ability to metabolize glycogen,…
Hypocatalasia is a rare genetic condition in dogs that affects their ability to produce the enzyme catalase, which helps protect cells from oxidative damage. A DNA test for hypocatalasia can…
Cats may suffer from metabolic disorders such as feline hyperlipidemia and certain inherited metabolic syndromes. Genetic testing aids in early detection.
Alpha Mannosidosis (AlphaMan) is a rare genetic disorder in cats caused by a deficiency of the enzyme alpha-mannosidase. This leads to the accumulation of complex sugars in cells, resulting in…
Dihydropyrimidinase Deficiency (DHP) is a rare genetic disorder that can affect cats, impacting their ability to properly break down certain amino acids. A DNA test for DHP helps identify carriers…
The DNA test for Gangliosidosis GM1 in cats detects mutations in the GLB1 gene responsible for this genetic disorder. GM1 gangliosidosis is a rare lysosomal storage disease that causes progressive…
Gangliosidosis GM2 is a genetic disorder that affects cats, caused by a deficiency in the enzyme needed to break down certain fats in the body. DNA testing can identify carriers…
The DNA test for Gangliosidosis GM2 in Domestic Shorthair cats detects a genetic mutation responsible for this rare lysosomal storage disorder. This condition affects the nervous system, leading to progressive…
Gangliosidosis GM2 is a genetic disorder found in Japanese Domestic cats, caused by a deficiency in the enzyme responsible for breaking down GM2 gangliosides. A DNA test can identify carriers…
Gangliosidosis GM2 in Korat cats is a genetic disorder caused by a deficiency of the enzyme responsible for breaking down GM2 gangliosides. This leads to the accumulation of toxic substances…
The Gangliosidosis GM2A (GM2A) DNA test in cats detects mutations associated with a rare lysosomal storage disorder. This genetic condition impairs the breakdown of GM2 gangliosides, leading to neurological symptoms.…
Hyperlipoproteinaemia (HLPA) in cats is a genetic condition characterized by elevated levels of lipoproteins in the blood. A DNA test can identify mutations associated with HLPA, helping veterinarians diagnose the…
Mucopolysaccharidosis I (MPS I) is a genetic disorder that can affect cats, caused by a deficiency in the enzyme alpha-L-iduronidase. This enzyme deficiency leads to the accumulation of complex sugars…
Mucopolysaccharidosis VI Variant 1 (MPSVI1) is a genetic disorder in cats caused by a mutation affecting the enzyme arylsulfatase B. This leads to the accumulation of glycosaminoglycans, resulting in progressive…
Mucopolysaccharidosis VI Variant 2 (MPSVI2) is a genetic disorder affecting cats, caused by a deficiency in the enzyme arylsulfatase B. This leads to the accumulation of complex sugars in cells,…
This page currently lists 56 genetic tests related to metabolic diseases, including 38 for Dog, 18 for Cat. These DNA tests may help identify inherited variants, clinically relevant genetic markers and species-specific screening options.
Genetic testing helps identify inherited variants associated with metabolic diseases, supports risk assessment and contributes to better breeding and screening decisions. It can also help veterinarians and owners interpret clinically relevant results more effectively.
Yes. Depending on the condition or biological pathway involved, genetic tests related to metabolic diseases may be available across dog, cat, horse or other species represented on this page.
Yes. When inherited variants are involved, metabolic diseases DNA tests can support breeding choices by helping identify carriers, affected animals or individuals with specific inherited risk profiles.
Metabolic diseases encompass a range of inherited disorders that interfere with the body's normal biochemical functions. These conditions can arise from genetic mutations affecting enzyme activity, leading to issues in energy metabolism, nutrient absorption, and waste processing. For breeders and veterinarians, understanding these diseases is essential for making informed decisions regarding breeding practices and health management. DNA testing plays a pivotal role in identifying genetic variants associated with metabolic disorders, allowing for early screening and intervention. This proactive approach can help mitigate the impact of these diseases on animal health. Species-specific screening is particularly important, as metabolic disorders can vary significantly between dogs, cats, and horses. By utilizing genetic testing, breeders can make informed choices to promote healthier offspring and enhance the overall well-being of their animals.
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