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 215+ disorders, plus genetic testing for all our adult dogs. We believe a healthy start makes for a healthy finish!
Open each toggle below and click on each disorder for more information.
Alexander Disease
(GFAP)
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD
(SPTBN2, Beagle Variant)
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia
(SEL1L, Finnish Hound Variant)
Cerebellar Hypoplasia
(VLDLR, Eurasier Variant)
Hereditary Ataxia, Cerebellar Degeneration
(RAB24, Old English Sheepdog and Gordon Setter Variant)
Fetal-Onset Neonatal Neuroaxonal Dystrophy
(MFN2, Giant Schnauzer Variant)
Hypomyelination and Tremors
(FNIP2, Weimaraner Variant)
Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome
(PLP1, English Springer Spaniel Variant)
L-2-Hydroxyglutaricaciduria, L2HGA
(L2HGDH, Staffordshire Bull Terrier Variant)
Alaskan Malamute Polyneuropathy, AMPN
(NDRG1 SNP)
Narcolepsy
(HCRTR2 Intron 4, Doberman Pinscher Variant)
Narcolepsy
(HCRTR2 Intron 6, Labrador Retriever Variant)
Narcolepsy
(HCRTR2 Exon 1, Dachshund Variant)
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD
(SERAC1 Exon 15, Kerry Blue Terrier Variant)
Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD
(SERAC1 Exon 4, Chinese Crested Variant)
Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV
(RAB3GAP1, Rottweiler Variant)
Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome, AMS
(GDNF-AS, Spaniel and Pointer Variant)
Sensory Neuropathy
(FAM134B, Border Collie Variant)
Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1
(LPN1, ARHGEF10)
Juvenile Myoclonic Epilepsy
(DIRAS1)
Neuroaxonal Dystrophy, NAD
(TECPR2, Spanish Water Dog Variant)
Neuroaxonal Dystrophy, NAD
(VPS11, Rottweiler Variant)
Leukodystrophy
(TSEN54 Exon 5, Standard Schnauzer Variant)
Spinocerebellar Ataxia
(SCN8A, Alpine Dachsbracke Variant)
Muscular Dystrophy
(DMD, Cavalier King Charles Spaniel Variant 1)
Muscular Dystrophy
(DMD, Golden Retriever Variant)
Limb Girdle Muscular Dystrophy
(SGCD, Boston Terrier Variant)
Ullrich-like Congenital Muscular Dystrophy
(COL6A3 Exon 10, Labrador Retriever Variant)
Centronuclear Myopathy, CNM
(PTPLA)
Myotonia Congenita
(CLCN1 Exon 7, Miniature Schnauzer Variant)
Myotonia Congenita
(CLCN1 Exon 23, Australian Cattle Dog Variant)
Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM
(MTM1, Labrador Retriever Variant)
Inflammatory Myopathy
(SLC25A12)
Nemaline Myopathy
(NEB, American Bulldog Variant)
Ullrich-like Congenital Muscular Dystrophy
(COL6A3 Exon 16, Labrador Retriever Variant)
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, German Shepherd Variant 1)
Factor VIII Deficiency, Hemophilia A
(F8 Exon 1, German Shepherd Variant 2)
Thrombopathia
(RASGRP1 Exon 5, Basset Hound Variant)
Thrombopathia
(RASGRP1 Exon 8, Landseer Variant)
Thrombopathia
(RASGRP1 Exon 5, American Eskimo Dog Variant)
Von Willebrand Disease Type III, Type III vWD
(VWF Exon 4, Terrier Variant)
Von Willebrand Disease Type III, Type III vWD
(VWF Exon 7, Shetland Sheepdog Variant)
Von Willebrand Disease Type II, Type II vWD
(VWF, Pointer Variant)
Canine Leukocyte Adhesion Deficiency Type I, CLAD I
(ITGB2, Setter Variant)
Canine Leukocyte Adhesion Deficiency Type III, CLAD III
(FERMT3, German Shepherd Variant)
Canine Elliptocytosis
(SPTB Exon 30)
Glanzmann’s Thrombasthenia Type I
(ITGA2B Exon 13, Great Pyrenees Variant)
Glanzmann’s Thrombasthenia Type I
(ITGA2B Exon 12, Otterhound Variant)
May-Hegglin Anomaly
(MYH9)
Congenital Macrothrombocytopenia
(TUBB1 Exon 1, Cairn and Norfolk Terrier Variant)
Prekallikrein Deficiency
(KLKB1 Exon 8)
Pyruvate Kinase Deficiency
(PKLR Exon 5, Basenji Variant)
Pyruvate Kinase Deficiency
(PKLR Exon 7, Labrador Retriever Variant)
Pyruvate Kinase Deficiency
(PKLR Exon 7, Pug Variant)
Pyruvate Kinase Deficiency
(PKLR Exon 7, Beagle Variant)
Pyruvate Kinase Deficiency
(PKLR Exon 10, Terrier Variant)
Trapped Neutrophil Syndrome, TNS
(VPS13B)
Methemoglobinemia
(CYB5R3)
Bernard-Soulier Syndrome, BSS
(GP9, Cocker Spaniel Variant)
Primary Ciliary Dyskinesia, PCD
(CCDC39 Exon 3, Old English Sheepdog Variant)
Primary Ciliary Dyskinesia, PCD
(NME5, Alaskan Malamute Variant)
Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID
(FAM83H Exon 5)
Canine Fucosidosis
(FUCA1)
Glycogen Storage Disease Type II, Pompe’s Disease, GSD II
(GAA, Finnish and Swedish Lapphund, Lapponian Herder Variant)
Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA
(G6PC, Maltese Variant)
Glycogen Storage Disease Type IIIA, GSD IIIA
(AGL, Curly Coated Retriever Variant)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA
(SGSH Exon 6, Dachshund Variant)
Mucopolysaccharidosis Type IIIA, Sanfilippo Syndrome Type A, MPS IIIA
(SGSH Exon 6, New Zealand Huntaway Variant)
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII
(GUSB Exon 5, Terrier Brasileiro Variant)
Mucopolysaccharidosis Type VII, Sly Syndrome, MPS VII
(GUSB Exon 3, German Shepherd Variant)
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency
(PFKM, Whippet and English Springer Spaniel Variant)
Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency
(PFKM, Wachtelhund Variant)
Lagotto Storage Disease
(ATG4D)
Neuronal Ceroid Lipofuscinosis 1, NCL 1
(PPT1 Exon 8, Dachshund Variant 1)
Neuronal Ceroid Lipofuscinosis 2, NCL 2
(TPP1 Exon 4, Dachshund Variant 2)
Neuronal Ceroid Lipofuscinosis, Cerebellar Ataxia, NCL4A
(ARSG Exon 2, American Staffordshire Terrier Variant)
Neuronal Ceroid Lipofuscinosis 5, NCL 5
(CLN5 Exon 4 SNP, Border Collie Variant)
Neuronal Ceroid Lipofuscinosis 6, NCL 6
(CLN6 Exon 7, Australian Shepherd Variant)
Neuronal Ceroid Lipofuscinosis 8, NCL 8
(CLN8 Exon 2, English Setter Variant)
Neuronal Ceroid Lipofuscinosis 7, NCL 7
(MFSD8, Chihuahua and Chinese Crested Variant)
Neuronal Ceroid Lipofuscinosis 8, NCL 8
(CLN8, Australian Shepherd Variant)
Neuronal Ceroid Lipofuscinosis 10, NCL 10
(CTSD Exon 5, American Bulldog Variant)
Neuronal Ceroid Lipofuscinosis 5, NCL 5
(CLN5 Exon 4 Deletion, Golden Retriever Variant)
Late-Onset Neuronal Ceroid Lipofuscinosis, NCL 12
(ATP13A2, Australian Cattle Dog Variant)
GM1 Gangliosidosis
(GLB1 Exon 15, Shiba Inu Variant)
GM1 Gangliosidosis
(GLB1 Exon 15, Alaskan Husky Variant)
GM1 Gangliosidosis
(GLB1 Exon 2, Portuguese Water Dog Variant)
GM2 Gangliosidosis
(HEXB, Poodle Variant)
GM2 Gangliosidosis
(HEXA, Japanese Chin Variant)
Globoid Cell Leukodystrophy, Krabbe disease
(GALC Exon 5, Terrier Variant)
Neuronal Ceroid Lipofuscinosis 8, NCL 8
(CLN8 Insertion, Saluki Variant)
Mucopolysaccharidosis IIIB, Sanfilippo Syndrome Type B, MPS IIIB
(NAGLU, Schipperke Variant)
Progressive Retinal Atrophy, rcd1
(PDE6B Exon 21, Irish Setter Variant)
Progressive Retinal Atrophy, CNGA
(CNGA1 Exon 9)
Progressive Retinal Atrophy, prcd
(PRCD Exon 1)
Progressive Retinal Atrophy, crd1
(PDE6B, American Staffordshire Terrier Variant)
Progressive Retinal Atrophy, PRA3
(FAM161A)
Day Blindness, Cone Degeneration, Achromatopsia
(CNGB3 Exon 6, German Shorthaired Pointer Variant)
Achromatopsia
(CNGA3 Exon 7, German Shepherd Variant)
Achromatopsia
(CNGA3 Exon 7, Labrador Retriever Variant)
Canine Multifocal Retinopathy, cmr1
(BEST1 Exon 2)
Canine Multifocal Retinopathy, cmr2
(BEST1 Exon 5, Coton de Tulear Variant)
Canine Multifocal Retinopathy, cmr3
(BEST1 Exon 10 Deletion, Finnish and Swedish Lapphund, Lapponian Herder Variant)
Primary Open Angle Glaucoma
(ADAMTS10 Exon 9, Norwegian Elkhound Variant)
Primary Open Angle Glaucoma
(ADAMTS10 Exon 17, Beagle Variant)
Primary Open Angle Glaucoma
(ADAMTS17 Exon 11, Basset Fauve de Bretagne Variant)
Primary Open Angle Glaucoma and Primary Lens Luxation
(ADAMTS17 Exon 2, Chinese Shar-Pei Variant)
Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts
(HSF4 Exon 9, Australian Shepherd Variant)
Primary Lens Luxation
(ADAMTS17)
Congenital Stationary Night Blindness
(RPE65, Briard Variant)
Congenital Stationary Night Blindness
(LRIT3, Beagle Variant)
Day Blindness, Cone Degeneration, Achromatopsia
(CNGB3 Deletion, Alaskan Malamute Variant)
Retina Dysplasia and/or Optic Nerve Hypoplasia
(SIX6 Exon 1, Golden Retriever Variant)
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption