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Health condition list

Ultimate peace of mind comes from testing for over 160 known genetic health conditions in 16 different areas, including:

Health

Clinical

Multidrug Sensitivity (MDR1)
Alanine Aminotransferase Activity (GPT)
Health

Blood

P2RY12 Defect (P2RY12)
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)
Thrombopathia (RASGRP2 Exon 8)
Von Willebrand Disease Type III (VWF Exon 4)
Factor VII Deficiency (F7 Exon 5)
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
Von Willebrand Disease Type II (VWF Exon 28)
Von Willebrand Disease Type I (VWF)
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 13)
Canine Elliptocytosis (SPTB Exon 30)
Glanzmann's Thrombasthenia Type I (ITGA2B Exon 12)
Prekallikrein Deficiency (KLKB1 Exon 8)
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)
Canine Leukocyte Adhesion Deficiency Type III (FERMT3)
Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)
May-Hegglin Anomaly (MYH9)
Pyruvate Kinase Deficiency (PKLR Exon 5)
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)
Pyruvate Kinase Deficiency (PKLR Exon 10)
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)
Ligneous Membranitis (PLG)
Trapped Neutrophil Syndrome (VPS13B)
Health

Hormones

Congenital hypothyroidism (TPO Variant 1)
Health

Immune

Severe Combined Immunodeficiency (PRKDC)
Complement 3 (C3) deficiency (C3)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)
Severe Combined Immunodeficiency (RAG1)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
Health

Eyes

Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd3 (PDE6A)
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)
Progressive Retinal Atrophy (PRA) Progressive rod-cone degeneration (PRCD Exon 1)
Progressive Retinal Atrophy (PRA) (CNGB1)
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
Progressive Retinal Atrophy (PRA) (CNGA1 Exon 9)
Progressive Retinal Atrophy (PRA) (SAG)
Progressive Retinal Atrophy (PRA) Golden Retriever PRA 2 (TTC8)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 2, crd2 (IQCB1)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 1, crd1 (PDE6B)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy, crd4/cord1 (RPGRIP1)
Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1)
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)
Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6)
Autosomal Dominant Progressive Retinal Atrophy (RHO)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Boston Terrier Variant)
Congenital stationary night blindness (RPE65)
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12)
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)
Macular Corneal Dystrophy (MCD) (CHST6)
Primary Lens Luxation (ADAMTS17)
Health

Multisystem

Gangliosidosis GM2 Gangliosidosis (HEXA)
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5)
Primary Ciliary Dyskinesia (CCDC39 Exon 3)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)
Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
Glycogen Storage Disease Type II, Pompe's Disease (GAA)
Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3)
Lagotto Storage Disease (ATG4D)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)
Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5)
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 8)
Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)
Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Exon 21)
Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)
Neuronal Ceroid Lipofuscinosis 1 (CLN5 Exon 4 Variant 1)
Neuronal Ceroid Lipofuscinosis (MFSD8)
Neuronal Ceroid Lipofuscinosis 1 (ARSG Exon 2)
Neuronal Ceroid Lipofuscinosis 8 (CLN8 Exon 2)
Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2)
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)
Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)
Neuronal Ceroid Lipofuscinosis (CLN8)
Neuronal Ceroid Lipofuscinosis (CLN5 Exon 4 Variant 2)
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)
Gangliosidosis GM1 Gangliosidosis (GLB1 Exon 2)
Gangliosidosis GM2 Gangliosidosis (HEXB Exon 3)
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
Health

Other Systems

Autosomal Recessive Amelogenesis Imperfecta (ENAM)
Persistent Mullerian Duct Syndrome (AMHR2)
Health

Kidney and Bladder

2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT)
Cystinuria Type II-A (SLC3A1)
Cystinuria Type I-A (SLC3A1)
Cystinuria Type II-B (SLC7A9)
Primary Hyperoxaluria (AGXT)
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9)
Protein Losing Nephropathy (NPHS1)
X-Linked Hereditary Nephropathy (COL4A5 Exon 35)
Polycystic Kidney Disease (PKD1)
Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 3)
Health

Skeletal

Hereditary Vitamin D-Resistant Rickets (VDR)
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)
Skeletal Dysplasia 2 (COL11A2)
Cleft Lip and/or Cleft Palate (ADAMTS20)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)
Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1)
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 (COL9A3)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)
Craniomandibular Osteopathy (CMO) (SLC7A2)
Health

Brain and Spinal Cord

Alexander Disease (GFAP)
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)
Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1)
Cerebellar Hypoplasia (VLDLR)
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)
Degenerative Myelopathy (SOD1A)
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)
Polyneuropathy (NDRG1 Exon 15)
Hypomyelination and Tremors (FNIP2)
L-2-Hydroxyglutaricaciduria (L2HGDH)
Polyneuropathy (NDRG1 Exon 4)
Neonatal Encephalopathy with Seizures (NEWS) (ATF2)
Narcolepsy (HCRTR2 Intron 6)
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)
Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)
Juvenile Laryngeal Paralysis and Polyneuropathy (RAB3GAP1)
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)
Health

Heart

Dilated Cardiomyopathy (PDK4)
Long QT Syndrome (KCNQ1)
Health

Muscular

Muscular Dystrophy Muscular Dystrophy (DMD Cavalier King Charles Spaniel Variant)
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
Centronuclear Myopathy (PTPLA)
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
Inherited Myopathy of Great Danes (BIN1)
Myotonia Congenita (CLCN1 Exon 23)
Exercise-Induced Collapse (DNM1)
Myotonia Congenita (CLCN1 Exon 7)
Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
Health

Metabolic

Malignant Hyperthermia (RYR1)
Pyruvate Dehydrogenase Deficiency (PDP1)
Hypocatalasia, Acatalasemia (CAT)
Health

Gastro-intestinal

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
Health

Neuro-muscular

Congenital Myasthenic Syndrome (COLQ)
Congenital Myasthenic Syndrome (CHAT)
Episodic Falling Syndrome (BCAN)
Health

Skin

Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)
Ichthyosis (SLC27A4)
Hereditary Footpad Hyperkeratosis (FAM83G)
Dystrophic Epidermolysis Bullosa (COL7A1)
Ichthyosis (PNPLA1)
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)
Hereditary Nasal Parakeratosis (SUV39H2)
Musladin-Lueke Syndrome (ADAMTSL2)

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