Tests for Newfoundland

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Below are the tests we currently offer for the Newfoundland

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Disease Panels

Newfoundland Panel

Best Price! Select this panel for only $143.00, a $165.00 value

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Cystinuria (Newfoundland Type)
Aliases: Type IA cystinuria
Degenerative Myelopathy (Common Variant)
Aliases: Canine degenerative myelopathy, DM
Thrombopathia (Newfoundland Type)
Aliases: Autoimmune thrombocytopenia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Thrombocytopathy, Thrombocytopenia

Disease Tests

Additional Disease Tests for Newfoundland

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Lafora Disease Blood, Tissue, or PPG Swab Kit Required
Aliases: Lafora's Disease, Myoclonus Epilepsy of Lafora, Progressive Myoclonus Epilepsy, PME
There are additional tests from breeds related to the Newfoundland.

Show tests for related breeds

Available Tests From Related Breeds

The breeds we know today have been selectively bred for from a few common ancestors. Breeds that were derived from common ancestors constitute a breed group. Because a breed group is genetically related, mutations and diseases in ancestors or within a breed put all breeds within that group at risk for the same inherited disorders. Therefore, we have provided you the diseases that occur in common ancestors and related breeds so that you can decide whether you wish to also exclude these diseases in your dog.
Click the test name to learn more Affected Breeds
Centronuclear Myopathy
Aliases: Hereditary myopathy of the Labrador Retriever, Type II muscle fiber deficiency, CNM
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
Aliases: CDDY with IVDD, CDPA, Hansen's Type I IVDD, Intervertebral Disc Disease
Cleft Palate and Syndactyly (Nova Scotia Duck Tolling Retriever Type)
Aliases: Cleft Lip/Palate and Syndactyly, CLPS
Collie Eye Anomaly
Aliases: Choroidal hypoplasia, CEA, CH
Cone Degeneration (Labrador Retriever Type)
Aliases: Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy
Congenital Myasthenic Syndrome (Golden Retriever Type)
Congenital Myasthenic Syndrome (Labrador Retriever Type)
Aliases: CMS
Copper Toxicosis (Labrador Retriever Type)
Aliases: Copper Hepatoxicosis, Copper Storage Disease, Copper Storage Disease Modifier, Copper Storage Hepatitis, Copper-associated Hepatopathy, Hepatic Copper Toxicosis, Menkes Gene Disease Modifier, Wilson Disease
Cystinuria (Labrador Retriever Type)
Aliases: Type IA cystinuria
Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
Aliases: Recessive dystrophic epidermolysis bullosa, DEB, EB, RDEB
Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2
Elliptocytosis
Exercise-Induced Collapse
Aliases: EIC
Glycogen Storage Disease IIIa
Aliases: GSD IIIa
Hereditary Nasal Parakeratosis (Labrador Retriever Type)
Aliases: HNPK
Hyperuricosuria
Aliases: Urolithiasis, HUU
Ichthyosis (Golden Retriever Type 1)
Ichthyosis (Golden Retriever Type 2)
Aliases: Nonepidermolytic ichthyosis, ICH2, NI
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
Aliases: Leonberger Laryngeal Paralysis and Polyneuropathy (LPPN3)
Macular Corneal Dystrophy (Labrador Retriever Type)
Aliases: MCD
Muscular Dystrophy (Golden Retriever Type)
Aliases: Duchenne-type muscular dystrophy, Dystrophin muscular dystrophy, DMD, GRMD
Myotonia Congenita (Labrador Retriever Type)
Aliases: MC
Myotubular Myopathy 1 (Labrador Retriever Type)
Aliases: X-linked myotubular myopathy, MTM1, XLMTM
Narcolepsy (Labrador Retriever Type)
Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type)
Aliases: Amaurotic Idiocy, Batten Disease, NCL, NCL5
Osteogenesis Imperfecta (Golden Retriever Type)
Aliases: Brittle bone disease, OI
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
Aliases: Progressive retinal atrophy - cord1, Progressive retinal atrophy - crd4, Progressive retinal atrophy - crd4/cord1, PRA-cord1, PRA-crd4, PRA-crd4/cord1
Progressive Retinal Atrophy, Golden Retriever 1
Aliases: GR-PRA1, GR1-PRA
Progressive Retinal Atrophy, Golden Retriever 2
Aliases: GR-PRA2, GR2-PRA
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
Aliases: PRA-PRCD, PRCD
Pyruvate Kinase Deficiency (Labrador Retriever Type)
Aliases: Pyruvate kinase deficiency of erythrocytes, PK deficiency
Retinal Dysplasia/Oculoskeletal Dysplasia 1
Aliases: Dwarfism with retinal dysplasia 1, Inherited retinal dysplasia, Oculoskeletal dysplasia 1, Retinal dysplasia, DRD1, OSD1, RD, RD/OSD
Skeletal Dysplasia 2
Aliases: Dwarfism, SD2
Stargardt Disease
Aliases: Juvenile Macular Degeneration, STGD
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2)
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Coat Color and Trait Tests

Paw Print Genetics offers testing for common coat colors and traits. Some genes have more than one mutation, such as those genes involved in Agouti and determining a brown coat color. The tests for those variants have been combined for simplicity in ordering. To learn more, just click any of the coat color or trait names below.