Health Screening
We offer the most comprehensive health screening on the market using the most up to date canine science available. Our full health panel (included in our Health and Behavior Analysis Kit and Breed, Behavior, and Health Plus Kit) covers 322 genetic markers associated with 183 health conditions. Our smaller panel (included in our Breed, Behavior, and Health Analysis Kit) covers 75 genetic markers associated with 32 of the most common canine health conditions. Below is a list of all of the health conditions included in our full health panel. Conditions in black are also included in our smaller health panel.
Behavioral
Canine Compulsive Disorder (CCD)
Blood
Factor VII Deficiency
Haemophilia A, or Factor VIII Deficiency
Haemophilia B, or Factor IX Deficiency
Macrothrombocytopenia
May-Hegglin Anomaly
Polycythemia
Postoperative hemorrhage, or Platelet Disorder of Swiss Mountain Dog (P2Y12 Receptor Platelet Disorder)
Prekallikrein Deficiency
Pyruvate Kinase Deficiency of Erythrocyte (PK Deficiency)
Scott Syndrome (CSS)
Thrombasthenia, or Glanzmann Thrombasthenia
Thrombopathia
Trapped Neutrophil Syndrome (TNS)
von Willebrand Disease, type 1
von Willebrand Disease, type 2
von Willebrand Disease, type 3
Cancer
Hemangiosarcoma
Histiocytic Sarcoma
Lymphoma
Malignant Melanoma
Mammary Tumors
Mast Cell Tumors
Squamous Cell Carcinoma of the Digit (SCCD)
Connective Tissue
Musladin-Lueke Syndrome
Dental
Amelogenesis Imperfecta
Dental Hypomineralization
Digestive
Inflammatory Bowel Disease (IBD)
Endocrine
Hypothyroidism
Pancreatic Acinar Atrophy (PAA)
Ears
Adult-onset Deafness
Deafness
Eyes
Achromatopsia-2
Autosomal-Dominant Progressive Retinal Atrophy (ADPRA)
Bardet-Biedl Syndrome 4
Collie Eye Anomaly
Cone Degeneration (cd), or Achromatopsia
Cone-rod Dystrophy 1 (crd1)
Cone-rod Dystrophy 2 (crd2)
Cone-rod Dystrophy, Standard Wire-Haired Dachshund (CRD^SWHD)
Degenerative myelopathy
Early Retinal Degeneration (erd)
Multifocal Retinopathy 1 (cmr1)
Multifocal Retinopathy 2 (cmr2)
Primary Closed Angle Glaucoma (PCAG)
Primary Hereditary Cataract (PHC)- Early Onset
Primary Lens Luxation (PLL)
Primary open angle glaucoma (POAG)
Progressive Retinal Atrophy (PRA)
Progressive Retinal Atrophy (PRA), type 3
Golden Retriever Progressive Retinal Atrophy, Type 1
Golden Retriever Progressive Retinal Atrophy, Type 2
Rod-cone Dysplasia 1 (rcd1)
Rod-cone Dysplasia 2 (rcd2)
Rod-cone Dysplasia 3 (rcd3)
Rod-cone Dysplasia 4 (rcd4)
Heart/ Circulatory System
Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)
Coronary Artery Disease
Cyclic Neutropenia (CN)
Dilated Cardiomyopathy (DCM)
Long QT Syndrome
Portosystemic Vascular Anomalies (PSVA)
Immune System
Autoinflammatory Disease (AID)
Histiocytosis, Malignant
IgA Deficiency
IgE Response to Dust Mites
Leukocyte Adhesion Deficiency, Type I (LAD1)
Leukocyte Adhesion Deficiency, Type III (LAD3)
Periodic Fever Syndrome
Primary Ciliary Dyskinesia (PCD)
Severe Combined Immunodeficiency Disease (SCID)
Kidneys/ Urinary
Cystinuria, Type IA
Cystinuria, Type IIA
Cystinuria, Type IIB
Hyperuricosuria and Hyperuricemia (huu)
Nephritis, or Alport Syndrome
Polycystic Kidney Disease (PKD)
Primary Hyperoxaluria Type I, or Oxalosis I
Liver
Gallbladder Mucoceles
Metabolism
Glycogen Storage Disease Ia
Glycogen Storage Disease IIIa
Glycogen Storage Disease VII
Hypocatalasia
Imerslund-Gräsbeck Syndrome (I-GS), or Selective Cobalamin Malabsorption; Megaloblastic Anemia 1 (MGA1)
Mucopolysaccharidosis I (MPS I)
Mucopolysaccharidosis VI (MPS VI)
Mucopolysaccharidosis VII (MPS VII)
Pyruvate Dehydrogenase Deficiency
Wilson Disease, COMMD1 Type
Muscular
Centronuclear Myopathy (CNM)
Congenital Myasthenic Syndrome (CMS)
Exercise-Induced Metabolic Myopathy
Exercise-Induced Collapse (EIC) Syndrome
Inherited Myopathy of Great Danes (IMGD)
Limb-girdle Muscular Dystrophy (LGMD)- Type 2F
Megaesophagus
Muscle Type Phosphofructokinase (M-PFK) Deficiency
Muscular Dystrophy, Duchenne Type, or Golden Retriever Muscular Dystrophy (GRMD)
Muscular Dystrophy, Limb-Girdle, Type 2F (LGMD2F)
Muscular Dystrophy, Ullrich type
Myotubular Myopathy 1, or X-linked Myotubular Myopathy (XLMTM)
Nemaline Myopathy
Nervous System
Acral Mutilation Syndrome
Bandera's Neonatal Ataxia (BNAt)
Canine Hereditary Ataxia
Ataxia, SEL1L-related
Spinocerebellar Ataxia (SCAIS)
Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1)
Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2)
Benign Familial Juvenile Epilepsy, or Remitting Focal Epilepsy
Cerebellar Cortical Degeneration
Fucosidosis
Gangliosidosis, GM1
Gangliosidosis, GM2, Type I (B variant), or Tay-Sachs Disease
Gangliosidosis, GM2, type II (Sandhoff or variant 0)
Hyperekplexia, or Startle Disease
Hypomyelination of the Central Nervous System
Idiopathic Epilepsy
Krabbe Disease, or Globoid Cell Leukodystrophy
L-2-hydroxyglutaricacidemia
Lagotto Storage Disease (LSD)
Leukoencephalomyelopathy (LEMP)
Narcolepsy
Necrotising Encephalopathy, or Alaskan Husky Encephalopathy (AHE)
Necrotizing Meningoencephalitis
Neonatal Cerebellar Cortical Degeneration
Neuroaxonal Dystrophy
Neuronal Ceroid Lipofuscinosis, Type 1
Neuronal Ceroid Lipofuscinosis, Type 2
Neuronal Ceroid Lipofuscinosis, Type 4A
Neuronal Ceroid Lipofuscinosis, Type 5
Neuronal Ceroid Lipofuscinosis, Type 6
Neuronal Ceroid Lipofuscinosis, Type 7
Neuronal Ceroid Lipofuscinosis, Type 8
Neuronal Ceroid Lipofuscinosis, Type 10
Neuronal Ceroid Lipofuscinosis, Type 12
Paroxysmal Dyskinesias (PxD)
Polyneuropathy
Polyneuropathy 1 (LPN1, or ILPN)
Polyneuropathy 2 (LPN2)
Sensory Neuropathy
Tremors, or Shaking Pup (SHP)
Pharmacology
Multiple Drug Resistance 1 (MDR1)
Poor Metabolizer of Cognitive Enhancer AC-3933
Response to Beta Blocker in Heart Failure
Reproductive
Cryptorchidism
Persistent Mullerian Duct Syndrome
Respiratory
Respiratory Distress Syndrome, or Acute Respiratory Distress Syndrome (ARDS)
Skeletal
Chiari-like Malformation
Chondrodysplasia (defect)
Intervertebral Disc Disease, Type I (IVDD1)
Craniomandibular Osteopathy (CMO), or Caffey Disease
Elbow Dysplasia
Hip Dysplasia
Oculoskeletal Dysplasia 1 (osd1)
Oculoskeletal Dysplasia 2 (osd2)
Osteoarthritis
Osteochondrodysplasia
Osteochondromatosis
Osteogenesis Imperfecta
Osteogenesis Imperfecta, Type III
Pituitary Dwarfism, LHX3-related
Skeletal Dysplasia (sd)
Spinal Dysraphism
Spondylocostal Dysostosis (SCD)
Van den Ende-Gupta Syndrome
Vitamin D-deficiency Rickets, Type II (HVDRR)
Skin
Anal Furunculosis
Atopic Dermatitis (cAD)
Cleft Lip with or without Cleft Palate (CL/P)
Cleft Palate 1 (CP1)
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKSID)
Dermatomyositis (DMS)
Ectodermal Dysplasia/Skin Fragility Syndrome (ED-SFS)
Epidermolysis Bullosa
Epidermolytic Hyperkeratosis
Exfoliative Cutaneous Lupus Erythematosus, chr5-related
Hereditary Nasal Parakeratosis (HNPK)
Ichthyosis
Lethal Acrodermatitis (LAD)
Palmoplantar Keratoderma, or Focal Non-Epidermolytic Palmoplantar Keratoderma (FNEPPK)
Symmetrical Onychomadesis
Other
Embryonic Lethality
We Offer 4 Different Test, Choose Which Kit Is Best For You
