At Midnight Schnauzers, our #1 priority is to provide you with a healthy, happy pet that you will enjoy for years to come. That’s why we offer a lifetime genetic health guarantee covering the following 165+ disorders, plus genetic testing for all our adult dogs. We believe a healthy start makes for a healthy finish! 

  • Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 15)
  • Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy (LGI2)
  • Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia (SEL1L)
  • Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration (SPTBN2)
  • Narcolepsy (HCRTR2 Intron 6)
  • Spinocerebellar Ataxia, Late-Onset Ataxia (CAPN1)
  • Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy (SLC19A3)
  • Spongy Degeneration with Cerebellar Ataxia 1 (SDCA1), SeSAME/EAST (KCNJ10)
  • Hypomyelination and Tremors (FNIP2)
  • Progressive Neuronal Abiotrophy (Canine Multiple System Degeneration) (SERAC1 Exon 4)
  • Degenerative Myelopathy (SOD1A)
  • L-2-Hydroxyglutaricaciduria (L2HGDH)
  • Polyneuropathy, NDRG1 Malamute Variant (NDRG1 Exon 4)
  • Spinocerebellar Ataxia with Myokymia and/or Seizures (KCNJ10)
  • Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome (GDNF-AS)
  • Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1 (LPN1, ARHGEF10)
  • Cerebellar Hypoplasia (VLDLR)
  • Spongy Degeneration with Cerebellar Ataxia 2 (SDCA2) (ATP1B2)
  • Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN2)
  • Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome (PLP)
  • Neonatal Encephalopathy with Seizures (NEWS) (ATF2)
  • Polyneuropathy, NDRG1 Greyhound Variant (NDRG1 Exon 15)
  • Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation (POANV) (RAB3GAP1, Rottweiler Variant)
  • Alexander Disease (GFAP)
  • Myotonia Congenita (CLCN1 Exon 23)
  • Inherited Myopathy of Great Danes (BIN1)
  • Myotonia Congenita (CLCN1 Exon 7)
  • Centronuclear Myopathy (PTPLA)
  • Myostatin Deficiency, Bully Whippet Syndrome (MSTN)
  • Muscular Dystrophy Muscular Dystrophy (DMD Golden Retriever Variant)
  • Myotubular Myopathy 1, X-linked Myotubular Myopathy (MTM1)
  • Exercise-Induced Collapse (DNM1)
  • Muscular Dystrophy Cavalier King Charles Spaniel Variant 1
  • Muscular Dystrophy Muscular Dystrophy (DMD Pembroke Welsh Corgi Variant )
  • Factor VIII Deficiency, Hemophilia A (F8 Exon 1, Shepherd Variant 2)
  • Ligneous Membranitis (PLG)
  • Von Willebrand Disease Type I (VWF)
  • Pyruvate Kinase Deficiency (PKLR Exon 7 Pug Variant)
  • Factor IX Deficiency, Hemophilia B (F9 Exon 7, Terrier Variant)
  • Pyruvate Kinase Deficiency (PKLR Exon 7 Labrador Variant)
  • Pyruvate Kinase Deficiency (PKLR Exon 5)
  • Thrombopathia (RASGRP2 Exon 5, American Eskimo Dog Variant)
  • P2Y12 Receptor Platelet Disorder (P2RY12)
  • May-Hegglin Anomaly (MYH9)
  • Thrombopathia (RASGRP2 Exon 8)
  • Factor VIII Deficiency, Hemophilia A (F8 Exon 11, Shepherd Variant 1)
  • Factor VIII Deficiency, Hemophilia A (F8 Exon 10, Boxer Variant)
  • Factor VII Deficiency (F7 Exon 5)
  • Congenital Macrothrombocytopenia (TUBB1 Exon 1, Cavalier King Charles Spaniel Variant)
  • Prekallikrein Deficiency (KLKB1 Exon 8)
  • Thrombopathia (RASGRP2 Exon 5, Basset Hound Variant)
  • Glanzmann’s Thrombasthenia Type I (ITGA2B Exon 12)
  • Pyruvate Kinase Deficiency (PKLR Exon 10)
  • Factor IX Deficiency, Hemophilia B (F9 Exon 7, Rhodesian Ridgeback Variant)
  • Pyruvate Kinase Deficiency (PKLR Exon 7 Beagle Variant)
  • Trapped Neutrophil Syndrome (VPS13B)
  • Cyclic Neutropenia, Gray Collie Syndrome (AP3B1 Exon 20)
  • Canine Leukocyte Adhesion Deficiency Type III (LAD3) (FERMT3)
  • Canine Elliptocytosis (SPTB Exon 30)
  • Von Willebrand Disease Type III (VWF Exon 4)
  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND) (FLCN Exon 7)
  • GM2 Gangliosidosis (HEXA)
  • Mucopolysaccharidosis Type I (IDUA)
  • Neuronal Ceroid Lipofuscinosis (MFSD8)
  • GM1 Gangliosidosis (GLB1 Exon 15 Shiba Inu Variant)
  • X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia (EDA Intron 8)
  • Globoid Cell Leukodystrophy, Krabbe disease (GALC Exon 5)
  • Neuronal Ceroid Lipofuscinosis 1 (PPT1 Exon 8)
  • Glycogen Storage Disease Type Ia, Von Gierke Disease (G6PC)
  • Neuronal Ceroid Lipofuscinosis (CLN5 Golden Retriever Variant)
  • Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID), Dry Eye Curly Coat Syndrome (FAM83H Exon 5)
  • Neuronal Ceroid Lipofuscinosis 2 (TPP1 Exon 4)
  • Glycogen Storage Disease Type IIIa (GSD IIIa) (AGL)
  • Neuronal Ceroid Lipofuscinosis (CLN8 Australian Shepherd Variant)
  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Whippet and English Springer Spaniel Variant)
  • Neuronal Ceroid Lipofuscinosis 8 (CLN8 English Setter Variant)
  • Primary Ciliary Dyskinesia (CCDC39 Exon 3)
  • Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 1)
  • Lagotto Storage Disease (ATG4D)
  • Neuronal Ceroid Lipofuscinosis 1, Cerebellar Ataxia – NCL-A (ARSG Exon 2)
  • Neuronal Ceroid Lipofuscinosis 6 (CLN6 Exon 7)
  • Canine Fucosidosis (FUCA1)
  • GM1 Gangliosidosis (GLB1 Exon 2)
  • GM1 Gangliosidosis (GLB1 Exon 15 Alaskan Husky Variant)
  • Glycogen Storage Disease Type II, Pompe’s Disease (GAA)
  • Adult-Onset Neuronal Ceroid Lipofuscinosis (ATP13A2)
  • Glycogen storage disease Type VII, Phosphofructokinase deficiency (PFKM Wachtelhund Variant)
  • GM2 Gangliosidosis (HEXB, Poodle Variant)
  • Neuronal Ceroid Lipofuscinosis 1 (CLN5 Border Collie Variant)
  • Neuronal Ceroid Lipofuscinosis 10 (CTSD Exon 5)
  • Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 3)
  • Mucopolysaccharidosis Type VII, Sly Syndrome (GUSB Exon 5)
  • Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A (SGSH Exon 6 Variant 2)
  • Progressive Retinal Atrophy Rod-cone dysplasia, rcd1a (PDE6B Exon 21 Sloughi Variant)
  • Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 Deletion)
  • Achromatopsia (CNGA3 Exon 7 German Shepherd Variant)
  • Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 2)
  • Canine Multifocal Retinopathy cmr3 (BEST1 Exon 10 SNP)
  • Canine Multifocal Retinopathy cmr1 (BEST1 Exon 2)
  • Progressive Retinal Atrophy – crd4/cord1 (RPGRIP1)
  • Glaucoma Primary Open Angle Glaucoma (ADAMTS17 Exon 11)
  • Progressive Retinal Atrophy – crd1 (PDE6B)
  • Canine Multifocal Retinopathy cmr2 (BEST1 Exon 5)
  • Progressive Retinal Atrophy – rcd1 Rod-cone dysplasia, rcd1 (PDE6B Exon 21 Irish Setter Variant)
  • Achromatopsia (CNGA3 Exon 7 Labrador Retriever Variant)
  • Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 9)
  • Progressive Retinal Atrophy (CNGB1)
  • Progressive Retinal Atrophy – prcd Progressive rod-cone degeneration (PRCD Exon 1)
  • Golden Retriever Progressive Retinal Atrophy 1 (SLC4A3)
  • Progressive Retinal Atrophy (SAG)
  • Macular Corneal Dystrophy (MCD) (CHST6)
  • Autosomal Dominant Progressive Retinal Atrophy (RHO)
  • Progressive Retinal Atrophy – rcd3 Rod-cone dysplasia, rcd3 (PDE6A)
  • Golden Retriever Progressive Retinal Atrophy 2 (TTC8)
  • Primary Lens Luxation (ADAMTS17)
  • Collie Eye Anomaly, Choroidal Hypoplasia (NHEJ1)
  • Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts (HSF4 Exon 9 Shepherd Variant)
  • Progressive Retinal Atrophy – crd2 (IQCB1)
  • Progressive Retinal Atrophy – CNGA (CNGA1 Exon 9)
  • Glaucoma Primary Open Angle Glaucoma (ADAMTS10 Exon 17)
  • Congenital stationary night blindness (RPE65)
  • Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 53)
  • Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption (CUBN Exon 8)
  • Dystrophic Epidermolysis Bullosa (COL7A1)
  • Ectodermal Dysplasia, Skin Fragility Syndrome (PKP1)
  • Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16)
  • Ichthyosis (PNPLA1)
  • Hereditary Footpad Hyperkeratosis (FAM83G)
  • Ichthyosis (NIPAL4)
  • Ichthyosis, Epidermolytic Hyperkeratosis (KRT10)
  • Hereditary Nasal Parakeratosis (SUV39H2)
  • Ichthyosis (SLC27A4)
  • Musladin-Lueke Syndrome (ADAMTSL2)
  • Hyperuricosuria and Hyperuricemia or Urolithiasis (SLC2A9)
  • Cystinuria Type I-A (SLC7A9)
  • Protein Losing Nephropathy (NPHS1)
  • X-Linked Hereditary Nephropathy (Samoyed Variant 2) (COL4A5 Exon 35)
  • Polycystic Kidney Disease (PKD1)
  • Cystinuria Type II-A (SLC3A1)
  • Cystinuria Type I-A (SLC3A1)
  • Primary Hyperoxaluria (AGXT)
  • Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy (COL4A4 Exon 3)
  • 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis (APRT)

Congenital Hypothyroidism (TPO, Tenterfield Terrier Variant)

  • Malignant Hyperthermia (RYR1)
  • Hypocatalasia, Acatalasemia (CAT)
  • Pyruvate Dehydrogenase Deficiency (PDP1)
  • Severe Combined Immunodeficiency (PRKDC)
  • X-linked Severe Combined Immunodeficiency (IL2RG Variant 2)
  • X-linked Severe Combined Immunodeficiency (IL2RG Variant 1)
  • Severe Combined Immunodeficiency (RAG1)
  • Complement 3 (C3) deficiency (C3)
  • Shar-Pei Autoinflammatory Disease (SPAID, Shar-Pei Fever) (MTBP)
  • Deafness and Vestibular Syndrome of Dobermans (DVDob, DINGS)
  • Persistent Mullerian Duct Syndrome (AMHR2)
  • Autosomal Recessive Amelogenesis Imperfecta (Italian Greyhound Variant)
  • Craniomandibular Osteopathy (CMO) (SLC37A2)
  • Hereditary Vitamin D-Resistant Rickets (VDR)
  • Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2)
  • Cleft Lip and/or Cleft Palate (ADAMTS20)
  • Osteochondrodysplasia, Skeletal Dwarfism (SLC13A1)
  • Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia (COL9A3, Labrador Retriever)
  • Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)
  • Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1)
  • Skeletal Dysplasia 2 (COL11A2)
  • Episodic Falling Syndrome (BCAN)
  • Congenital Myasthenic Syndrome (CHAT)
  • Congenital Myasthenic Syndrome (COLQ)
  • Long QT Syndrome (KCNQ1)
  • Dilated Cardiomyopathy (PDK4)
  • MDR1 Drug Sensitivity (MDR1)
  • Alanine Aminotransferase (ALT) Activity (GPT)