Acral Mutilation Syndrome
Alexander Disease
Ataxia, Cerebellar
Ataxia, Cerebellar, KCNIP4-related
Ataxia, Cerebellar, KCNJ10-related
Ataxia, Cerebellar, Progressive Early-Onset
Ataxia, Cerebellar, RAB24-related
Ataxia, Spinocerebellar, CAPN1-related
Ataxia, Spinocerebellar, SCN8A-related
Cerebellar Cortical Degeneration
Degenerative Myelopathy
Epilepsy, Benign Familial Juvenile
Gangliosidosis, GM1
Gangliosidosis, GM2, Type I
Hereditary Sensory Autonomic Neuropathies
Krabbe Disease
Laryngeal Paralysis and Polyneuropathy
Leukodystrophy, TSEN54-related
Leukoencephalomyelopathy
Narcolepsy
Neonatal Encephalopathy with Seizures
Neuroaxonal Dystrophy, Juvenile
Neuroaxonal Dystrophy, PLA2G6-related
Neuroaxonal Dystrophy, VPS11-related
Neuronal Ceroid Lipofuscinosis, 1
Neuronal Ceroid Lipofuscinosis, 10
Neuronal Ceroid Lipofuscinosis, 4A
Neuronal Ceroid Lipofuscinosis, 5
Neuronal Ceroid Lipofuscinosis, 8
Neuropathy, Sensory
Polyneuropathy, NDRG1-related
Polyneuropathy, SBF2-related
Spinocerebellar Ataxia
Tremor, X-linked

B-Cell Lymphoma
Combined Haemangiosarcoma and B-Cell Lymphoma
Haemangiosarcoma
Histiocytic Sarcoma
Mammary Tumours
Mast Cell Tumours
Osteosarcoma
Renal Cystadenocarcinoma and Nodular Dermatofibrosis
T-Zone Lymphoma

Ectodermal Dysplasia
Ehlers-Danlos Syndrome, Classic Type, 1
Ehlers-Danlos Syndrome, Type VII (Dermatosparaxis)
Epidermolysis Bullosa, Junctionalis, LAMA3-related
Epidermolysis Bullosa, Simplex, PLEC-related
Hyperkeratosis, Palmoplantar
Ichthyosis, ASPRV1-related
Ichthyosis, SLC27A4-related
Lethal Acrodermatitis
Musladin-Lueke Syndrome
Nasal Parakeratosis
Verrucous Epidermal Keratinocytic Nevi

Gastric Dilatation Volvulus
Inflammatory Bowel Disease

Deafness
Deafness, Bilateral, and Vestibular Dysfunction
Upper Airway Syndrome

Achromatopsia 2
Canine Retinopathy
Coat Colour, Oculocutaneous Albinism, OCA2-related
Eye Malformation, Congenital
Glaucoma, Primary Open Angle, ADAMTS10-related
Glaucoma, Primary Open Angle, ADAMTS17-related
Goniodysgenesis and Severe Goniodysgenesis
Lens Luxation
Macular Corneal Dystrophy
Multifocal Retinopathy 1
Multifocal Retinopathy 2
Progressive Retinal Atrophy
Progressive Retinal Atrophy, Basenji
Progressive Retinal Atrophy, Miniature Schnauzer, Type 1
Progressive Retinal Atrophy, NECAP1-related
Progressive Rod-Cone Degeneration
Rod-Cone Dysplasia 1
X-linked Progressive Retinal Atrophy 1, XLPRA1-related

Cardiomyopathy
Cardiomyopathy, Dilated, PLN-related
Degenerative Mitral Valve Disease
Mitral Valve Prolapse

Anti-Lu. Longipalpis SGH IgG
Leukocyte Adhesion Deficiency, Type I
Periodic Fever Syndrome
Severe Combined Immunodeficiency Disease, Autosomal
Severe Combined Immunodeficiency Disease, Autosomal, T Cell-Negative, B Cell-Negative, NK Cell-Positive
Symmetrical Lupoid Onychodystrophy

Ectopic Ureters
Nephritis, X-linked
Primary Hyperoxaluria Type I

Addison’s Disease
Alanine Amino Transferase Level
Beta-mannosidosis
Blood Glucose Level
Congenital Dyshormonogenic Hypothyroidism with Goiter
Fructosamine Level
Glycogen Storage Disease Ia
Glycogen Storage Disease II
Glycogen Storage Disease VII
Hypocatalasia
Hypophosphatasia
Hypothyroidism
Intestinal Cobalamin Malabsorption, AMN-related
Intestinal Cobalamin Malabsorption, CUBN-related
Menkes Disease
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Neurodegenerative Vacuolar Storage Disease
Pyruvate Kinase Deficiency of Erythrocyte
Xanthinuria, Type I
Xanthinuria, Type II

Anterior Cruciate Ligament Rupture
Canine Degenerative Myelopathy
Canine Hip Dysplasia
Centronuclear Myopathy
Chondrodysplasia, Disproportionate Short-Limbed
Congenital Muscular Dystrophy
Cranial Cruciate Ligament Disease
Craniomandibular Osteopathy
Dwarfism, Disproportionate
Dyskinesia, Paroxysmal, PIGN-related
Elbow Dysplasia
Exercise-Induced Collapse
Golden Retriever Muscular Dystrophy
Inflammatory Myopathy, SLC25A12-related
Muscular Dystrophy-Dystroglycanopathy
Muscular Dystrophy, COL6A3-related
Muscular Dystrophy, Duchenne
Muscular Dystrophy, Ullrich Type
Myasthenic Syndrome, Congenital
Myasthenic Syndrome, Congenital, COLQ-related
Myotonia
Myotubular Myopathy 1
Nemaline Myopathy, NEB-related
Osteoarthritis
Osteogenesis Imperfecta, COL1A2-related
Osteogenesis Imperfecta, SERPINH1-related, Dachshund
Skeletal Dysplasia 2
X-linked Facial Dysmorphia

4-Hydroxyproline Level
Threonine level

Dental Hypomineralization

Male Reproductive Traits
Persistent Mullerian Duct Syndrome

Canine Idiopathic Pulmonary Fibrosis
Ciliary Dyskinesia, Primary
Laryngeal Paralysis
Respiratory Distress Syndrome
Surfactant Metabolism Dysfunction, Pulmonary