Health condition list

Ultimate peace of mind comes from testing for over 170+ known genetic health conditions in 16 different areas, including:

  • Clinical

    MDR1 Drug Sensitivity

    (MDR1)

    Alanine Aminotransferase (ALT) Activity

    (GPT)
  • Blood

    P2Y12 Receptor Platelet Disorder

    (P2RY12)

    Factor IX Deficiency, Hemophilia B

    (F9 Exon 7, Terrier Variant)

    Factor IX Deficiency, Hemophilia B

    (F9 Exon 7, Rhodesian Ridgeback Variant)

    Factor VII Deficiency

    (F7 Exon 5)

    Factor VIII Deficiency, Hemophilia A

    (F8 Exon 10, Boxer Variant)

    Factor VIII Deficiency, Hemophilia A

    (F8 Exon 11, Shepherd Variant 1)

    Factor VIII Deficiency, Hemophilia A

    (F8 Exon 1, Shepherd Variant 2)

    Thrombopathia

    (RASGRP2 Exon 5, Basset Hound Variant)

    Thrombopathia

    (RASGRP2 Exon 8)

    Thrombopathia

    (RASGRP2 Exon 5, American Eskimo Dog Variant)

    Von Willebrand Disease Type III

    (VWF Exon 4)

    Von Willebrand Disease Type I

    (VWF)

    Von Willebrand Disease Type II

    (VWF)

    Canine Leukocyte Adhesion Deficiency Type III (LAD3)

    (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 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)
  • 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)
  • Hormones

    Congenital Hypothyroidism

    (TPO, Tenterfield Terrier Variant)
  • Eyes

    Progressive Retinal Atrophy - rcd1

    Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)

    Progressive Retinal Atrophy

    Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)

    Progressive Retinal Atrophy - rcd3

    Rod-cone dysplasia, rcd3 (PDE6A)

    Progressive Retinal Atrophy - CNGA

    (CNGA1 Exon 9)

    Progressive Retinal Atrophy - prcd

    Progressive rod-cone degeneration (PRCD Exon 1)

    Progressive Retinal Atrophy

    (CNGB1)

    Progressive Retinal Atrophy

    (SAG)

    Golden Retriever Progressive Retinal Atrophy 1

    (SLC4A3)

    Golden Retriever Progressive Retinal Atrophy 2

    (TTC8)

    Progressive Retinal Atrophy - crd1

    (PDE6B)

    Progressive Retinal Atrophy - crd2

    (IQCB1)

    Progressive Retinal Atrophy - crd4/cord1

    (RPGRIP1)

    Collie Eye Anomaly, Choroidal Hypoplasia

    (NHEJ1)

    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 Deletion)

    Canine Multifocal Retinopathy

    cmr3 (BEST1 Exon 10 SNP)

    Glaucoma

    Primary Open Angle Glaucoma (ADAMTS10 Exon 9)

    Glaucoma

    Primary Open Angle Glaucoma (ADAMTS10 Exon 17)

    Glaucoma

    Primary Open Angle Glaucoma (ADAMTS17 Exon 11)

    Glaucoma

    Primary Open Angle Glaucoma (ADAMTS17 Exon 2)

    Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts

    (HSF4 Exon 9 Shepherd Variant)

    Primary Lens Luxation

    (ADAMTS17)

    Congenital stationary night blindness

    (RPE65)

    Macular Corneal Dystrophy (MCD)

    (CHST6)
  • Multisystem

    Glycogen Storage Disease Type Ia, Von Gierke Disease

    (G6PC)

    Primary Ciliary Dyskinesia

    (CCDC39 Exon 3)

    Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome

    (FAM83H Exon 5)

    X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia

    (EDA Intron 8)

    Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)

    (FLCN Exon 7)

    Canine Fucosidosis

    (FUCA1)

    Glycogen Storage Disease Type II, Pompe's Disease

    (GAA)

    Glycogen Storage Disease Type IIIa (GSD IIIa)

    (AGL)

    Mucopolysaccharidosis Type I

    (IDUA)

    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 Whippet and English Springer Spaniel Variant)

    Glycogen storage disease Type VII, Phosphofructokinase deficiency

    (PFKM Wachtelhund Variant)

    Lagotto Storage Disease

    (ATG4D)

    Neuronal Ceroid Lipofuscinosis 1

    (PPT1 Exon 8)

    Neuronal Ceroid Lipofuscinosis 2

    (TPP1 Exon 4)

    Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia - NCL-A

    (ARSG Exon 2)

    Neuronal Ceroid Lipofuscinosis 1

    (CLN5 Border Collie Variant)

    Neuronal Ceroid Lipofuscinosis 6

    (CLN6 Exon 7)

    Neuronal Ceroid Lipofuscinosis 8

    (CLN8 English Setter Variant)

    Neuronal Ceroid Lipofuscinosis

    (MFSD8)

    Neuronal Ceroid Lipofuscinosis

    (CLN8 Australian Shepherd Variant)

    Neuronal Ceroid Lipofuscinosis 10

    (CTSD Exon 5)

    Neuronal Ceroid Lipofuscinosis

    (CLN5 Golden Retriever Variant)

    Adult-Onset Neuronal Ceroid Lipofuscinosis

    (ATP13A2)

    GM1 Gangliosidosis

    (GLB1 Exon 15 Shiba Inu Variant)

    GM1 Gangliosidosis

    (GLB1 Exon 15 Alaskan Husky Variant)

    GM1 Gangliosidosis

    (GLB1 Exon 2)

    GM2 Gangliosidosis

    (HEXB, Poodle Variant)

    GM2 Gangliosidosis

    (HEXA)

    Globoid Cell Leukodystrophy, Krabbe disease

    (GALC Exon 5)
  • Kidney and Bladder

    2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis

    (APRT)

    Cystinuria Type I-A

    (SLC3A1)

    Cystinuria Type II-A

    (SLC3A1)

    Cystinuria Type I-A

    (SLC7A9)

    Hyperuricosuria and Hyperuricemia or Urolithiasis

    (SLC2A9)

    Polycystic Kidney Disease

    (PKD1)

    Primary Hyperoxaluria

    (AGXT)

    Protein Losing Nephropathy

    (NPHS1)

    X-Linked Hereditary Nephropathy (Samoyed Variant 2)

    (COL4A5 Exon 35)

    Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy

    (COL4A4 Exon 3)
  • Other Systems

    Autosomal Recessive Amelogenesis Imperfecta

    (Italian Greyhound Variant)

    Persistent Mullerian Duct Syndrome

    (AMHR2)

    Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)

    Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever)

    (MTBP)
  • Brain and Spinal Cord

    Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy

    (SLC19A3)

    Alexander Disease

    (GFAP)

    Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration

    (SPTBN2)

    Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia

    (SEL1L)

    Cerebellar Hypoplasia

    (VLDLR)

    Spinocerebellar Ataxia, Late-Onset Ataxia

    (CAPN1)

    Spinocerebellar Ataxia with Myokymia and/or Seizures

    (KCNJ10)

    Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy

    (LGI2)

    Degenerative Myelopathy

    (SOD1A)

    Fetal-Onset Neonatal Neuroaxonal Dystrophy

    (MFN2)

    Hypomyelination and Tremors

    (FNIP2)

    Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome

    (PLP)

    L-2-Hydroxyglutaricaciduria

    (L2HGDH)

    Neonatal Encephalopathy with Seizures (NEWS)

    (ATF2)

    Polyneuropathy, NDRG1 Greyhound Variant

    (NDRG1 Exon 15)

    Polyneuropathy, NDRG1 Malamute Variant

    (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)

    Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation (POANV)

    (RAB3GAP1, Rottweiler Variant)

    Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome

    (GDNF-AS)

    Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1

    (LPN1, ARHGEF10)

    Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST

    (KCNJ10)

    Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2)

    (ATP1B2)
  • Heart

    Dilated Cardiomyopathy

    (PDK4)

    Long QT Syndrome

    (KCNQ1)
  • Muscular

    Muscular Dystrophy

    Cavalier King Charles Spaniel Variant 1

    Muscular Dystrophy

    Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )

    Muscular Dystrophy

    Muscular Dystrophy (DMD Golden Retriever Variant)

    Centronuclear Myopathy

    (PTPLA)

    Exercise-Induced Collapse

    (DNM1)

    Inherited Myopathy of Great Danes

    (BIN1)

    Myostatin Deficiency, Bully Whippet Syndrome

    (MSTN)

    Myotonia Congenita

    (CLCN1 Exon 7)

    Myotonia Congenita

    (CLCN1 Exon 23)

    Myotubular Myopathy 1, X-linked Myotubular Myopathy

    (MTM1)
  • Metabolic

    Hypocatalasia, Acatalasemia

    (CAT)

    Pyruvate Dehydrogenase Deficiency

    (PDP1)

    Malignant Hyperthermia

    (RYR1)
  • Gastrointestinal

    Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption

    (CUBN Exon 53)

    Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption

    (CUBN Exon 8)
  • Neuromuscular

    Congenital Myasthenic Syndrome

    (CHAT)

    Congenital Myasthenic Syndrome

    (COLQ)

    Episodic Falling Syndrome

    (BCAN)
  • Skin & Connective Tissues

    Dystrophic Epidermolysis Bullosa

    (COL7A1)

    Ectodermal Dysplasia, Skin Fragility Syndrome

    (PKP1)

    Ichthyosis, Epidermolytic Hyperkeratosis

    (KRT10)

    Ichthyosis

    (PNPLA1)

    Ichthyosis

    (SLC27A4)

    Ichthyosis

    (NIPAL4)

    Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita

    (KRT16)

    Hereditary Footpad Hyperkeratosis

    (FAM83G)

    Hereditary Nasal Parakeratosis

    (SUV39H2)

    Musladin-Lueke Syndrome

    (ADAMTSL2)
  • Skeletal

    Cleft Lip and/or Cleft Palate

    (ADAMTS20)

    Hereditary Vitamin D-Resistant Rickets

    (VDR)

    Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia

    (COL9A3, Labrador Retriever)

    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)

    Craniomandibular Osteopathy (CMO)

    (SLC37A2)

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