Full list of over 170 health conditions we test for in 16 different areas:
Blood
Thrombopathia (RASGRP2 Exon 8)
Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)
Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)
P2Y12 Receptor Platelet Disorder (P2RY12)
Glanzmann’s Thrombasthenia Type I (ITGA2B Exon 12)
Von Willebrand Disease Type II, Type II vWD (VWF)
May-Hegglin Anomaly (MYH9)
Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
Von Willebrand Disease Type I (VWF)
Canine Elliptocytosis (SPTB Exon 30)
Canine Leukocyte Adhesion Deficiency Type III, LAD3 (FERMT3)
Prekallikrein Deficiency (KLKB1 Exon 8)
Von Willebrand Disease Type III, Type III vWD (VWF Exon 4)
Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)
Trapped Neutrophil Syndrome (VPS13B)
Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)
Methemoglobinemia CYB5R3
Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
Pyruvate Kinase Deficiency (PKLR Exon 5)
Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)
Factor VII Deficiency (F7 Exon 5)
Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
Ligneous Membranitis, LM (PLG)
Platelet factor X receptor deficiency, Scott Syndrome (TMEM16F)
Pyruvate Kinase Deficiency (PKLR Exon 10)
Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)
Other Systems
Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever (MTBP)
Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia (Italian Greyhound Variant)
Persistent Mullerian Duct Syndrome, PMDS (AMHR2)
Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS (MYO7A)
Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia (Parson Russell Terrier Variant)
Eyes
Progressive Retinal Atrophy, crd2 (IQCB1)
Primary Lens Luxation (ADAMTS17)
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2)
Progressive Retinal Atrophy, crd1 (PDE6B)
Progressive Retinal Atrophy, rcd1 rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
Collie Eye Anomaly, Choroidal Hypoplasia, CEA (NHEJ1)
Progressive Retinal Atrophy (SAG)
Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)
Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)
Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)
Progressive Retinal Atrophy, prcd Progressive rod-cone degeneration (PRCD Exon 1)
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts 
Autosomal Dominant Progressive Retinal Atrophy (RHO)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)
Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)
Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)
Progressive Retinal Atrophy, rcd3 rod-cone dysplasia, rcd3 (PDE6A)
Progressive Retinal Atrophy (CNGB1)
Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)
Progressive Retinal Atrophy, CNGA (CNGA1 Exon 9)
Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1 (SLC4A3)
Progressive Retinal Atrophy – crd4/cord1 (RPGRIP1)
Congenital Stationary Night Blindness (RPE65)
Macular Corneal Dystrophy, MCD (CHST6)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)
Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)
Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)
Muscular
Centronuclear Myopathy (PTPLA)
Myotonia Congenita (CLCN1 Exon 7)
Inherited Myopathy of Great Danes (BIN1)
Myotonia Congenita (CLCN1 Exon 23)
Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
Exercise-Induced Collapse (DNM1)
Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
Myostatin Deficiency, Bully Whippet Syndrome (MSTN)
Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1, Labrador Variant)
Muscular Dystrophy Cavalier King Charles Spaniel Variant 1
Multisystem
Primary Ciliary Dyskinesia, PCD (CCDC39 Exon 3)
GM1 Gangliosidosis (GLB1 Exon 2)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 1)
Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Tibetan Terrier Variant)
GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)
Neuronal Ceroid Lipofuscinosis 2, NCL 2 (TPP1 Exon 4)
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 3)
Canine Fucosidosis (FUCA1)
GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)
Lagotto Storage Disease (ATG4D)
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID (FAM83H Exon 5)
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Whippet and English Springer Spaniel Variant)
Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA (G6PC)
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant)
Neuronal Ceroid Lipofuscinosis 1, NCL 1 (CLN5 Border Collie Variant)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA (SGSH Exon 6 Variant 2)
Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia, NCL-A (ARSG Exon 2)
Neuronal Ceroid Lipofuscinosis 6, NCL 6 (CLN6 Exon 7)
Mucopolysaccharidosis Type I, MPS I (IDUA)
Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND (FLCN Exon 7)
Neuronal Ceroid Lipofuscinosis 10, NCL 10 (CTSD Exon 5)
Late-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2, Australian Cattle Dog Variant)
Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
Glycogen Storage Disease Type IIIA, GSD IIIA (AGL)
Neuronal Ceroid Lipofuscinosis (MFSD8)
GM2 Gangliosidosis (HEXB, Poodle Variant)
X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant)
Neuronal Ceroid Lipofuscinosis 8, NCL 8 (CLN8 English Setter Variant)
Neuronal Ceroid Lipofuscinosis 1, NCL 1 (PPT1 Exon 8)
Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII (GUSB Exon 5)
Glycogen Storage Disease Type II, Pompe’s Disease, GSD II (GAA)
GM2 Gangliosidosis (HEXA)
Skin & Connective Tissues
Ichthyosis (PNPLA1)
Ichthyosis (SLC27A4)
Dystrophic Epidermolysis Bullosa (COL7A1)
Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)
Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)
Ichthyosis (NIPAL4)
Musladin-Lueke Syndrome (ADAMTSL2)
Bald Thigh Syndrome (IGFBP5)
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)
Hereditary Nasal Parakeratosis (SUV39H2)
Hereditary Footpad Hyperkeratosis (FAM83G)
Brain and Spinal Cord
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1 (LPN1, ARHGEF10)
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD (SPTBN2)
Narcolepsy (HCRTR2 Intron 6)
Neuroaxonal Dystrophy, NAD (Spanish Water Dog Variant)
Neuroaxonal Dystrophy, NAD (Rottweiler Variant)
L-2-Hydroxyglutaricaciduria, L2HGA (L2HGDH)
Spongy Degeneration with Cerebellar Ataxia 2, SDCA2 (ATP1B2)
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 15)
Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)
Neonatal Encephalopathy with Seizures, NEWS (ATF2)
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)
Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV (RAB3GAP1, Rottweiler Variant)
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD (SERAC1 Exon 4)
Alexander Disease (GFAP)
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)
Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome, AMS (GDNF-AS)
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)
Hypomyelination and Tremors (FNIP2)
Spinocerebellar Ataxia, Late-Onset Ataxia, LoSCA (CAPN1)
Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15)
Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)
Cerebellar Hypoplasia (VLDLR)
Spongy Degeneration with Cerebellar Ataxia 1, SDCA1, SeSAME/EAST Syndrome (KCNJ10)
Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
Degenerative Myelopathy, DM (SOD1A)
Heart
Dilated Cardiomyopathy, DCM1 (PDK4)
Long QT Syndrome (KCNQ1)
Dilated Cardiomyopathy, DCM2 (TTN)
Skeletal
Hereditary Vitamin D-resistant Rickets (VDR)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)
Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD (FGF4 retrogene – CFA12)
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)
Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10)
Craniomandibular Osteopathy, CMO (SLC37A2)
Skeletal Dysplasia 2, SD2 (COL11A2)
Cleft Lip and/or Cleft Palate (ADAMTS20)
Musculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia, OSD1 Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1)
Metabolic
Malignant Hyperthermia (RYR1)
Hypocatalasia, Acatalasemia (CAT)
Pyruvate Dehydrogenase Deficiency (PDP1)
Kidney and Bladder
Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU (SLC2A9)
2,8-Dihydroxyadenine Urolithiasis, 2,8-DHA Urolithiasis (APRT)
Polycystic Kidney Disease, PKD (PKD1)
Protein Losing Nephropathy, PLN (NPHS1)
Cystinuria Type II-A (SLC3A1)
Primary Hyperoxaluria (AGXT)
Cystinuria Type I-A (SLC3A1)
Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN (COL4A4 Exon 3)
X-Linked Hereditary Nephropathy, XLHN (COL4A5 Exon 35, Samoyed Variant 2)
Cystinuria Type II-B (SLC7A9)
Neuromuscular
Episodic Falling Syndrome (BCAN)
Congenital Myasthenic Syndrome (COLQ)
Congenital Myasthenic Syndrome (CHAT)
Immune
Severe Combined Immunodeficiency (RAG1)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)
Severe Combined Immunodeficiency (PRKDC)
X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
Complement 3 Deficiency, C3 Deficiency (C3)
Gastrointestinal
Lundehund Syndrome (LEPREL1)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
Clinical
MDR1 Drug Sensitivity (MDR1)
Angiotensin-Converting Enzyme Activity (ACE)
Alanine Aminotransferase Activity (GPT)
Hormones
Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)