Metabolic disorders
Beta-mannosidosis
Ciliary dyskinesia, CCDC39-related
Ciliary dyskinesia, NME5-related
Erythrocytic pyruvate kinase (PK) deficiency
Exercise induced metabolic myopathy
Fucosidosis
Gangliosidosis, GM1
Gangliosidosis, GM2, type I
Gangliosidosis, GM2, type II
Glycogen storage disease, type IA
Glycogen storage disease, type II
Glycogen storage disease, type IIIA
Glycogen storage disease, type VII
Hypocatalasia (Acatalasemia)
Menkes disease
Mucopolysaccharidosis I
Mucopolysaccharidosis IIIA
Mucopolysaccharidosis IIIB
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Neuronal ceroid lipofuscinosis, ARSG-related
Neuronal ceroid lipofuscinosis, ATP13A2-related
Neuronal ceroid lipofuscinosis, CLN5-related
Neuronal ceroid lipofuscinosis, CLN6-related
Neuronal ceroid lipofuscinosis, CLN8-related
Neuronal ceroid lipofuscinosis, CTSD-related
Neuronal ceroid lipofuscinosis, MFSD8-related
Neuronal ceroid lipofuscinosis, PPT1-related
Neuronal ceroid lipofuscinosis, TPP1-related
Pyruvate dehydrogenase deficiency
Succinic semialdehyde dehydrogenase deficiency
Wilson's disease, ATP7B-related
Wilson's disease, COMMD1-related
Xanthinuria, type I
Xanthinuria, type II
Recommended by top vets with decades of experience
21 breeds
64 genetic health markers
50 genetic trait markers
