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.

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)

Narcolepsy

(HCRTR2 Intron 4, Doberman Pinscher Variant)

Narcolepsy

(HCRTR2 Intron 6, Labrador Retriever Variant)

Narcolepsy

(HCRTR2 Exon 1, Dachshund Variant)

Sensory Neuropathy

(FAM134B, Border Collie Variant)

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)

Myotonia Congenita

(CLCN1 Exon 7, Miniature Schnauzer Variant)

Myotonia Congenita

(CLCN1 Exon 23, Australian Cattle Dog Variant)

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 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 7, Shetland Sheepdog 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)

Congenital Macrothrombocytopenia

(TUBB1 Exon 1, Cairn and Norfolk Terrier Variant)

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)

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)

Glycogen Storage Disease Type II, Pompe’s Disease, GSD II

(GAA, Finnish and Swedish Lapphund, Lapponian Herder Variant)

Glycogen Storage Disease Type IIIA, GSD IIIA

(AGL, Curly Coated Retriever 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)

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)
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Progressive Retinal Atrophy, rcd1

(PDE6B Exon 21, Irish Setter Variant)

Progressive Retinal Atrophy, crd1

(PDE6B, American Staffordshire Terrier Variant)

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, 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)

Day Blindness, Cone Degeneration, Achromatopsia

(CNGB3 Deletion, Alaskan Malamute Variant)

Retina Dysplasia and/or Optic Nerve Hypoplasia

(SIX6 Exon 1, Golden Retriever Variant)

Dystrophic Epidermolysis Bullosa

(COL7A1, Golden Retriever Variant)

Dystrophic Epidermolysis Bullosa

(COL7A1, Central Asian Shepherd Dog Variant)

Ectodermal Dysplasia, Skin Fragility Syndrome

(PKP1, Chesapeake Bay Retriever Variant)

Ichthyosis, ICH1

(PNPLA1, Golden Retriever Variant)

Ichthyosis

(SLC27A4, Great Dane Variant)

Ichthyosis

(NIPAL4, American Bulldog Variant)

Hereditary Footpad Hyperkeratosis

(FAM83G, Terrier and Kromfohrlander Variant)

Hereditary Footpad Hyperkeratosis

(DSG1, Rottweiler Variant)

Oculocutaneous Albinism, OCA

(SLC45A2, Small Breed Variant)

Ehlers Danlos

(ADAMTS2, Doberman Pinscher Variant)

Congenital Hypothyroidism

(TPO, Tenterfield Terrier Variant)

Congenital Hypothyroidism

(TPO, Rat, Toy, Hairless Terrier Variant)

Congenital Myasthenic Syndrome, CMS

(CHAT, Old Danish Pointing Dog Variant)

Congenital Myasthenic Syndrome, CMS

(COLQ, Labrador Retriever Variant)

Congenital Myasthenic Syndrome, CMS

(CHRNE, Jack Russell Terrier Variant)

Congenital Myasthenic Syndrome, CMS

(COLQ, Golden Retriever Variant)

Myasthenia Gravis-Like Syndrome

(CHRNE, Heideterrier Variant)

Laryngeal Paralysis

(RAPGEF6, Miniature Bull Terrier Variant)

Dilated Cardiomyopathy, DCM1

(PDK4, Doberman Pinscher Variant 1)

Dilated Cardiomyopathy, DCM2

(TTN, Doberman Pinscher Variant 2)

Dilated Cardiomyopathy, DCM

(RBM20, Schnauzer Variant)
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