Health condition list

Ultimate peace of mind comes from testing for over 160 known genetic health conditions in 17 different areas, including:

Health

Clinical

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

Blood

Coagulopathy P2RY12 Defect (P2RY12)
Coagulopathy Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)
Coagulopathy Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
Coagulopathy Factor VII Deficiency (F7 Exon 5)
Coagulopathy Factor VIII Deficiency, Hemophilia A (F8 Exon 10)
Coagulopathy Factor VIII Deficiency, Hemophilia A (F8 Exon 11)
Coagulopathy Factor VIII Deficiency, Hemophilia A (F8 Exon 1)
Coagulopathy Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
Coagulopathy Thrombopathia (RASGRP2 Exon 8)
Coagulopathy Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
Coagulopathy Von Willebrand Disease Type II (VWF Exon 28)
Coagulopathy Von Willebrand Disease Type III (VWF Exon 4)
Canine Leucocyte Adhesion Deficiency Type I (ITGB2)
Canine Leucocyte Adhesion Deficiency Type III (FERMT3)
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
Canine elliptocytosis (SPTB Exon 30)
Cyclic neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)
Glanzmann's thrombasthenia Type I (ITGA2B Exon 13)
Glanzmann's thrombasthenia Type I (ITGA2B Exon 12)
May-Hegglin Anomaly (MYH9)
Prekallikrein Deficiency (KLKB1 Exon 8)
Pyruvate kinase deficiency (PKLR Exon 5)
Pyruvate kinase deficiency (PKLR Exon 7 Labrador Variant)
Pyruvate kinase deficiency (PKLR Exon 7 Pug Variant)
Pyruvate kinase deficiency (PKLR Exon 7 Beagle Variant)
Pyruvate kinase deficiency (PKLR Exon 10)
Trapped Neutrophil Syndrome (VPS13B)
Ligneous Membranitis (PLG)
Health

Hormones

Congenital hypothyroidism (TPO Variant 1)
Health

Immune

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

Eyes

Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)
Progressive Retinal Atrophy (PRA) Rod-cone dysplasia, rcd3 (PDE6A)
Progressive Retinal Atrophy (PRA) (CNGA1 Exon 9)
Progressive Retinal Atrophy (PRA) Progressive rod-cone degeneration (PRCD Exon 1)
Progressive Retinal Atrophy (PRA) (CNGB1)
Progressive Retinal Atrophy (PRA) (SAG)
Progressive Retinal Atrophy (PRA) Golden Retriever PRA 1 (SLC4A3)
Progressive Retinal Atrophy (PRA) Golden Retriever PRA 2 (TTC8)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 1, crd1 (PDE6B)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy 2, crd2 (IQCB1)
Progressive Retinal Atrophy (PRA) Cone-rod dystrophy, crd4 (RPGRIP1)
Day blindness, Achromatopsia, Cone Degeneration (CNGB3 Exon 6)
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)
Autosomal Dominant Progressive Retinal Atrophy (RHO)
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Variant 1)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Variant 2)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 12)
Hereditary cataracts, Early-onset cataracts, Juvenile cataracts (HSF4 Exon 9 Boston Terrier Variant)
Primary Lens Luxation (ADAMTS17)
Congenital stationary night blindness (RPE65)
Health

Kidney and Bladder

2,8-Dihydroxyadenine (2,8-DHA) urolithiasis (APRT)
Cystinuria Type I-A (SLC3A1)
Cystinuria Type II-A (SLC3A1)
Cystinuria Type II-B (SLC7A9)
Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9)
Polycystic Kidney Disease (PKD1)
Primary Hyperoxaluria (AGXT)
Protein Losing Nephropathy (NPHS1)
Protein Losing Nephropathy (KIRREL2)
Protein Losing Nephropathy X-Linked Hereditary Nephropathy (COL4A5 Exon 35)
Protein Losing Nephropathy Familial Nephropathy, Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 30)
Protein Losing Nephropathy Familial Nephropathy, Autosomal Recessive Hereditary Nephropathy (COL4A4 Exon 3)
Health

Multisystem

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

Other Systems

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

Brain and Spinal Cord

Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
Alexander disease (GFAP)
Cerebellar disease Cerebellar abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)
Cerebellar disease Cerebellar ataxia, Progressive early-onset cerebellar ataxia (SEL1L)
Cerebellar disease Cerebellar hypoplasia (VLDLR)
Cerebellar disease Late-onset ataxia, Spinocerebellar ataxia (CAPN1)
Cerebellar disease Spinocerebellar ataxia with myokymia and/or seizures (KCNJ10)
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)
Degenerative myelopathy (SOD1 Exon 2)
Axonal Disease Fetal-onset neonatal neuroaxonal dystrophy (MFN2)
Axonal Disease Hypomyelination and Tremor (FNIP2)
Axonal Disease Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)
L-2-Hydroxyglutaricacidemia (L2HGDH)
Neonatal Encephalopathy with Seizures (ATF2)
Polyneuropathy (NDRG1 Exon 15)
Polyneuropathy (NDRG1 Exon 4)
Narcolepsy (HCRTR2 Intron 6)
Progressive neuronal abiotrophy, Canine Multiple System Degeneration (SERAC1 Exon 15)
Progressive neuronal abiotrophy, Canine Multiple System Degeneration (SERAC1 Exon 4)
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 Pembroke Welsh Corgi Variant )
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
Exercise-induced collapse (DNM1)
Inherited myopathy of Great Danes (BIN1)
Bully Whippet Syndrome (MSTN)
Myotonia congenita (CLCN1 Exon 7)
Myotonia congenita (CLCN1 Exon 23)
Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
Health

Metabolic

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

Gastro-intestinal

Imerslund-Grasbeck Syndrome, Selective cobalamin malabsorption (CUBN Exon 53)
Imerslund-Grasbeck Syndrome, Selective cobalamin malabsorption (CUBN Exon 8)
Health

Liver

Gallbladder mucoceles (ABCB4)
Health

Neuro-muscular

Congenital Myasthenic Syndrome (CHAT)
Congenital Myasthenic Syndrome (COLQ)
Episodic falling syndrome (BCAN)
Health

Skin

Dystrophic epidermolysis bullosa (COL7A1)
Ectodermal dysplasia or Skin Fragility Syndrome (PKP1)
Ichthyosis, Epidermolytic hyperkeratosis (KRT10)
Ichthyosis (PNPLA1)
Ichthyosis (SLC27A4)
Focal non-epidermolytic palmoplantar keratoderma, pachyonychia congenita (KRT16)
Hereditary Footpad Hyperkeratosis (FAM83G)
Hereditary nasal parakeratosis (SUV39H2)
Musladin-Lueke syndrome (ADAMTSL2)
Health

Skeletal

Cleft lip with or without cleft palate (ADAMTS20)
Hereditary Vitamin D-Resistant Rickets (VDR)
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 1 (COL9A3)
Osteogenesis imperfecta, Brittle bone disease (COL1A2)
Osteogenesis imperfecta, Brittle bone disease (SERPINH1)
Osteogenesis imperfecta, Brittle bone disease (COL1A1)
Osteochondrodysplasia, Skeletal dwarfism (SLC13A1)
Skeletal Dysplasia 2 (COL11A2)

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