

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)