Paw Print Genetics - Disease Test Catalog

A large part of our work involves research.

In order to determine which diseases should be tested for each breed, we've read and analyzed the published literature. Most diseases are found in a specific breed, but your dog could be at risk for diseases in a related breed.

Below are the diseases for which testing is available.

Select a disease to get more information, find common symptoms, and read about helpful testing tips. You can alternatively search for diseases specific to your particular breed.

A

Acral Mutilation Syndrome: Pain Insensitivity, Sensory Neuropathy, AMS, SN
Acute Respiratory Distress Syndrome: Familial Acute Respiratory Distress Syndrome, ARDS
Adult Paroxysmal Dyskinesia: Paroxysmal Dyskinesia, cPxD, PxD
Afibrinogenemia (Dachshund Type)
Alaskan Husky Encephalopathy: Subacute necrotizing encephalomyelopathy, AHE
Alaskan Malamute Polyneuropathy: Hereditary polyneuropathy of Alaskan Malamutes, Inherited polyneuropathy, AMPN
Amelogenesis Imperfecta (Italian Greyhound Type): Autosomal recessive amelogenesis imperfecta, Familial enamel hypoplasia, AI, ARAI
Amelogenesis Imperfecta (Parson Russell Terrier Type)
Amelogenesis Imperfecta (Samoyed Type): Autosomal recessive amelogenesis imperfecta, enamel hypoplasia, AI, ARAI
Ataxia (Norwegian Buhund Type)

B

Benign Familial Juvenile Epilepsy: BFJE
Bernard-Soulier Syndrome: Bernard-Soulier Syndrome Type C, BSS

C

Canine Multiple System Degeneration (Chinese Crested Type): CMSD
Canine Multiple System Degeneration (Kerry Blue Terrier Type): Progressive neuronal abiotrophy, CMSD, PNA
Canine Scott Syndrome: Platelet Procoagulant Deficiency, Scott Syndrome, CSS
Cardiomyopathy and Juvenile Mortality
Catalase Deficiency: Acatalasemia, Hypocatalasemia, Hypocatalasia, Takahara's Disease
Centronuclear Myopathy: Hereditary myopathy of the Labrador Retriever, Type II muscle fiber deficiency, CNM
Cerebellar Ataxia (Finnish Hound Type): Progressive early onset ataxia
Cerebellar Ataxia (Spinone Italiano Type): Blood Sample Required and 3-4 Week Processing Time from Sample Receipt
Canine Hereditary Ataxia, HA
Cerebellar Ataxia 1 (Belgian Shepherd Type): Spongy Degeneration with Cerebellar Ataxia 1, SDCA
Cerebellar Ataxia 2 (Belgian Shepherd Type): Spongy degeneration with cerebellar ataxia 2, SBCA2
Cerebellar Cortical Degeneration: Cerebellar Abiotrophy, CA, CCD
Cerebellar Degeneration: Canine Hereditary Ataxia, Cerebellar Abiotrophy, CA, HA
Charcot-Marie-Tooth Disease
Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound Type): Dwarfism
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA): CDDY with IVDD, CDPA, Hansen's Type I IVDD, Intervertebral Disc Disease
Cleft Palate and Syndactyly (Nova Scotia Duck Tolling Retriever Type): Cleft Lip/Palate and Syndactyly, CLPS
Coagulation Factor VII Deficiency: Factor VII deficiency, Hypoproconvertinemia
Collie Eye Anomaly: Choroidal hypoplasia, CEA, CH
Complement 3 Deficiency: C3 deficiency, Complement component 3 deficiency
Cone Degeneration: Achromatopsia, Cone degeneration 1, Day blindness, Hemeralopia, Rod monochromacy, CD, CD1
Cone Degeneration (German Shepherd Dog Type): Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy, CD
Cone Degeneration (German Shorthaired Pointer Type): Achromatopsia, Cone degeneration 2, Day blindness, Hemeralopia, Rod monochromacy, CD2
Cone Degeneration (Labrador Retriever Type): Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy
Congenital Hypothyroidism with Goiter (Spanish Water Dog Type): CHG
Congenital Hypothyroidism with Goiter (Terrier Type): CHG
Congenital Macrothrombocytopenia (Cairn and Norfolk Terrier Type): Macrothrombocytopenia, Macrothrombocytosis, Thrombocytopenia, MTC
Congenital Methemoglobinemia: Familial Congenital Methemoglobinemia
Congenital Myasthenic Syndrome (Golden Retriever Type)
Congenital Myasthenic Syndrome (Jack Russell Terrier Type): CMS
Congenital Myasthenic Syndrome (Labrador Retriever Type): CMS
Congenital Myasthenic Syndrome (Old Danish Pointer Type): CMS
Congenital Stationary Night Blindness: Hereditary retinal dystrophy, Leber congenital amaurosis, Retinal pigment epithelial dystrophy, CSNB, LCA
Copper Storage Disease: Copper hepatoxicosis, Copper storage hepatitis, Copper toxicosis, Copper-associated hepatopathy, Hepatic copper toxicosis, Wilson disease, BTCT, CT
Copper Toxicosis (Labrador Retriever Type): Copper Hepatoxicosis, Copper Storage Disease, Copper Storage Disease Modifier, Copper Storage Hepatitis, Copper-associated Hepatopathy, Hepatic Copper Toxicosis, Menkes Gene Disease Modifier, Wilson Disease
Craniomandibular Osteopathy: CMO
Cyclic Neutropenia: Cyclic hematopoiesis, Gray collie syndrome, CH, CN
Cystinuria (Australian Cattle Dog Type): Autosomal dominant cystinuria, Type IIA cystinuria
Cystinuria (Labrador Retriever Type): Type IA cystinuria
Cystinuria (Miniature Pinscher Type)
Cystinuria (Newfoundland Type): Type IA cystinuria
Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 2 and 3): Non-Type I Cystinuria

D

Dandy-Walker-Like Malformation: Cerebellar Ataxia, Cerebellar Hypoplasia, Dandy-Walker-like Malformation, VLDLR-Associated Cerebellar Hypoplasia, DWLM
Darier Disease and Associated Infundibular Cyst Formation: Canine Darier Disease, Darier-White disease, keratosis follicularis
Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Variant 1: Congenital hearing and vestibular disorder, DINGS, DVD
Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Variant 2
Degenerative Myelopathy (Bernese Mountain Dog Variant): Canine Degenerative Myelopathy, DM, SOD1B
Degenerative Myelopathy (Common Variant): Canine degenerative myelopathy, DM
Degenerative Myelopathy Early-Onset Risk Modifier (Pembroke Welsh Corgi Type)
Dental Hypomineralization
Dermatomyositis: List Price $170 and 3-4 Week Processing Time from Sample Receipt
Juvenile Dermatomyositis, DMS, JDM
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis
Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 1): DCM
Dilated Cardiomyopathy (Doberman Pinscher Type Risk Factor, Variant 2): DCM
Dilated Cardiomyopathy (Schnauzer Type): DCM
Dry Eye Curly Coat Syndrome: Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, CKSID
Dystrophic Epidermolysis Bullosa (Basset Hound Type): DEB
Dystrophic Epidermolysis Bullosa (Golden Retriever Type): Recessive dystrophic epidermolysis bullosa, DEB, EB, RDEB

E

Early Onset Adult Deafness (Rhodesian Ridgeback Type): Early onset deafness, EOAD
Early Retinal Degeneration: Progressive retinal atrophy-erd, Retinal photoreceptor dysplasia, ERD
Early-Onset Epilepsy (Parson Russell Terrier Type)
Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
Ectodermal Dysplasia, X-Linked (Dachshund Type): Hypohidrotic Ectodermal Dysplasia, XLHED
Ectodermal Dysplasia, X-Linked (Shepherd Type): Anhidrotic Ectodermal Dysplasia, Congenital hypotrichosis, Ectodermal dysplasia, X-linked ectodermal dysplasia, X-linked hypohidrotic ectodermal dysplasia, XHED, XLED
Ehlers-Danlos Syndrome (Doberman Pinscher Type)
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 1
Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2
Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2): EDS
Elliptocytosis
Epidermolytic Hyperkeratosis: Ichthyosis
Episodic Falling Syndrome: Collapsing Cavaliers syndrome, Exercise-induced paroxysmal hypertonicity, Falling Cavaliers syndrome, Sudden collapse syndrome, EFS
Exercise-Induced Collapse: EIC
Exfoliative Cutaneous Lupus Erythematosus (ECLE)

F

Factor XI Deficiency: Coagulation Factor XI Deficiency
Familial Nephropathy (Cocker Spaniel Type): Hereditary nephropathy, Nephropathy, FN, HN
Familial Nephropathy (English Springer Spaniel Type): Hereditary nephropathy, Nephropathy, FN, HN
Fanconi Syndrome: Fanconi's syndrome, Paradoxic glucosuria
Fucosidosis: Alpha Fucosidosis

G

GM1 Gangliosidosis (Alaskan Husky Type)
GM1 Gangliosidosis (Portuguese Water Dog Type)
GM1 Gangliosidosis (Shiba Inu Type)
GM2 Gangliosidosis (Japanese Chin Type): Sandhoff disease, Tay-Sachs disease, Type 0 gangliosidosis
GM2 Gangliosidosis (Poodle Type): Sandhoff disease, Type 0 gangliosidosis
GM2 Gangliosidosis (Shiba Inu Type)
Gallbladder Mucoceles: Hepatobiliary disease, Mucinous cholecystitis, Mucinous hyperplasia
Glanzmann's Thrombasthenia (Great Pyrenees Type): Thrombasthenia, Thrombasthenic thrombopathia, GT
Glanzmann's Thrombasthenia (Otterhound Type): Thrombasthenia, Thrombasthenic thrombopathia, GT
Glaucoma (Border Collie Type): Goniodysgenesis, Primary Closed Angle Glaucoma, PCAG
Globoid Cell Leukodystrophy (Irish Setter Type): Galactocerebrosidase deficiency, Krabbe disease, GLD
Globoid Cell Leukodystrophy (Terrier Type): Galactocerebrosidase deficiency, Krabbe disease, GLD
Glycogen Storage Disease IIIa: GSD IIIa
Glycogen Storage Disease Ia: Von Gierke disease, GSD Ia, GSD1a
Glycogen Storage Disease VII (Wachtelhund Type): Phosphofructokinase deficiency, GSD VII, PFK deficiency
Glycogen Storage Disease VII, PFK Deficiency: Phosphofructokinase deficiency, GSD VII, PFK deficiency
Greyhound Polyneuropathy: Hereditary neuropathy

H

Hemophilia A (Boxer Type): Factor VIII Deficiency
Hemophilia A (German Shepherd Dog, Type 1): Factor VIII Deficiency
Hemophilia A (German Shepherd Dog, Type 2): Factor VIII deficiency
Hemophilia A (Rhodesian Ridgeback Type): Factor VIII deficiency
Hemophilia B (Cairn Terrier Type): Christmas disease, Factor IX deficiency
Hemophilia B (Lhasa Apso Type): Christmas disease, Factor IX deficiency
Hemophilia B (Rhodesian Ridgeback Type): Christmas disease, Factor IX deficiency
Hereditary Ataxia (Australian Shepherd Type)
Hereditary Cataracts: Early onset cataracts, Juvenile cataracts, HC, JC
Hereditary Cataracts (Australian Shepherd Type): Early onset cataracts, Juvenile cataracts, HC, HSF4, JC
Hereditary Cataracts (Wirehaired Pointing Griffon Type)
Hereditary Footpad Hyperkeratosis (Irish Terrier and Kromfohrländer type): "corny feet", Digital hyperkeratosis, DH, HFH
Hereditary Footpad Hyperkeratosis (Rottweiler Type)
Hereditary Nasal Parakeratosis (Greyhound Type): HNPK
Hereditary Nasal Parakeratosis (Labrador Retriever Type): HNPK
Hereditary Nephritis (Samoyed Type): Alport syndrome, Samoyed hereditary glomerulopathy, X-linked nephritis, AS, HN, XLHN
Hyperuricosuria: Urolithiasis, HUU
Hypomyelination (Weimaraner Type): Hypomyelination Syndrome, Shaky puppy syndrome, Spinal cord hypomyelination, Tremors, HS, HYM

I

Ichthyosis (American Bulldog Type): Autosomal recessive congenital ichthyosis, Nonepidermolytic ichthyosis, ARCI
Ichthyosis (Golden Retriever Type 1)
Ichthyosis (Golden Retriever Type 2): Nonepidermolytic ichthyosis, ICH2, NI
Ichthyosis (Great Dane Type)
Ichthyosis (Jack Russell Terrier Type): Lamellar Ichthyosis, LI
Inflammatory Myopathy (Shepherd Type)
Inherited Myopathy of Great Danes: Central core myopathy, IMGD
Intestinal Cobalamin Malabsorption (Australian Shepherd Type): Amnionless Deficiency, Cobalamin Deficiency, Imerslund-Grasbeck Syndrome, Vitamin B12 Deficiency
Intestinal Cobalamin Malabsorption (Beagle Type): Cobalamin Deficiency, Cubilin deficiency, Imerslund-Grasbeck syndrome, Vitamin B12 Deficiency, I-GS
Intestinal Cobalamin Malabsorption (Border Collie Type): Cobalamin deficiency, Cubilin deficiency, Imerslund-Grasbeck syndrome, I-GS
Intestinal Cobalamin Malabsorption (Giant Schnauzer Type): Amnionless Deficiency, Cobalamin Deficiency, Imerslund-Grasbeck Syndrome, Vitamin B12 Deficiency, I-GS
Intestinal Lipid Malabsorption

J

Junctional Epidermolysis Bullosa (Australian Shepherd Type)
Juvenile Laryngeal Paralysis and Polyneuropathy (Black Russian Terrier Type): Neuronal Vacuolation, Polyneuropathy with Ocular Abnormalities, JLPP, POANV
Juvenile Myoclonic Epilepsy (Rhodesian Ridgeback Type): Myoclonic Epilepsy, JME

L

L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type): L-2-hydroxyglutaricacidemia, Organic aciduria, L-2-HGA
L-2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type): L-2-hydroxyglutaricacidemia, Organic aciduria, L-2-HGA
Lafora Disease: Blood, Tissue, or PPG Swab Kit Required
Lafora's Disease, Myoclonus Epilepsy of Lafora, Progressive Myoclonus Epilepsy, PME
Lagotto Storage Disorder: Neurodegenerative Vacuolar Storage Disease, LSD
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3): Leonberger Laryngeal Paralysis and Polyneuropathy (LPPN3)
Late Onset Ataxia: Spinocerebellar ataxia, LOA, SCA
Lethal Acrodermatitis: LAD
Leukocyte Adhesion Deficiency, Type I: Canine Leukocyte Adhesion Deficiency, CLAD, LAD-I
Leukocyte Adhesion Deficiency, Type III: Canine leukocyte adhesion deficiency, Leukocyte/Platelet adhesion defect, CLAD, LAD-III
Leukoencephalomyelopathy: Canine Leukoencephalomyelopathy, LEMP
Ligneous Membranitis: LM
Limb-Girdle Muscular Dystrophy (Dachshund Type): limb-girdle muscular dystrophy 2D, LGMD, LGMD2
Lundehund Syndrome: LS

M

Macular Corneal Dystrophy (Labrador Retriever Type): MCD
May-Hegglin Anomaly: MHA
Microphthalmia (Soft Coated Wheaten Terrier Type): Canine Congenital Eye Disease, Multiple ocular defects with microphthalmia, MAC
Mucopolysaccharidosis I (Boston Terrier Type): Alpha-L-iduronidase deficiency, Hurler syndrome, Scheie syndrome, MPS I
Mucopolysaccharidosis I (Plott Hound Type): Alpha-L-iduronidase deficiency, Hurler syndrome, Scheie syndrome, MPS I
Mucopolysaccharidosis IIIA (Dachshund Type): Sanfilippo syndrome type A, MPS IIIA
Mucopolysaccharidosis IIIA (New Zealand Huntaway Type): Sanfilippo syndrome type A, MPS IIIA
Mucopolysaccharidosis IIIB (Schipperke Type): MPS IIIB
Mucopolysaccharidosis VI (Miniature Schnauzer Type): MPS VI
Mucopolysaccharidosis VII (Brazilian Terrier Type): Beta-glucuronidase deficiency, Sly Syndrome, MPS VII
Mucopolysaccharidosis VII (Shepherd Type): Beta-glucuronidase deficiency, Sly Syndrome, MPS VII
Multidrug Resistance 1: Ivermectin sensitivity, MDR1 gene defect, Multidrug sensitivity, MDR1
Multifocal Retinopathy 1: Canine multifocal retinopathy 1, CMR1
Multifocal Retinopathy 2: Canine multifocal retinopathy 2, CMR2
Multifocal Retinopathy 3: Canine multifocal retinopathy 3, CMR3
Muscular Dystrophy (Golden Retriever Type): Duchenne-type muscular dystrophy, Dystrophin muscular dystrophy, DMD, GRMD
Musladin-Lueke Syndrome: Chinese Beagle Syndrome, MLS
Myostatin Deficiency (Whippet Type): Bully Whippet
Myotonia Congenita (Australian Cattle Dog Type): Congenital myotonia, Inherited myotonia, Myotonia, Myotonia hereditaria
Myotonia Congenita (Labrador Retriever Type): MC
Myotonia Congenita (Schnauzer Type): Congenital myotonia, Inherited myotonia, Myotonia, Myotonia hereditaria
Myotubular Myopathy 1 (Boykin Spaniel Type): X-linked Myotubular Myopathy, MTM1, XLMTM
Myotubular Myopathy 1 (Labrador Retriever Type): X-linked myotubular myopathy, MTM1, XLMTM
Myotubular Myopathy 1 (Rottweiler Type): X-linked Myotubular Myopathy, MTM1, XLMTM

R

Recurrent Inflammatory Pulmonary Disease: IPD
Renal Cystadenocarcinoma and Nodular Dermatofibrosis: Renal cancer syndrome
Retinal Dysplasia/Oculoskeletal Dysplasia 1: Dwarfism with retinal dysplasia 1, Inherited retinal dysplasia, Oculoskeletal dysplasia 1, Retinal dysplasia, DRD1, OSD1, RD, RD/OSD
Retinal Dysplasia/Oculoskeletal Dysplasia 2: Dwarfism with retinal dysplasia 2, Inherited retinal dysplasia, Oculoskeletal dysplasia 2, Retinal dysplasia, DRD2, OSD2, RD, RD/OSD2

S

Sensory Neuropathy (Border Collie Type): SN
Severe Combined Immunodeficiency Disease (Terrier Type): Combined immunodeficiency disease, SCID
Severe Combined Immunodeficiency Disease (Wetterhoun Type): Combined immunodeficiency disease, SCID
Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type): XSCID
Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type): XSCID
Shar-Pei Autoinflammatory Disease: Familial Renal Amyloidosis, Hock Fever, Periodic Fever, Shar-Pei Fever, Swollen Hock Syndrome, SPAID
Skeletal Dysplasia 2: Dwarfism, SD2
Spinal Dysraphism: SD
Spinocerebellar Ataxia (Alpine Dachsbrake Type): SA
Spinocerebellar Ataxia (Terrier Type): Spinocerebellar ataxia and myokymia, SCA
Spondylocostal Dysostosis: Comma defect, SCD
Stargardt Disease: Juvenile Macular Degeneration, STGD
Startle Disease: Hyperekplexia
Subacute Necrotizing Encephalopathy (Yorkshire Terrier Type): juvenile-onset necrotizing encephalopathy, Leigh-Like Subacute Necrotizing Encephalopathy, SNE

T

Thrombopathia (American Eskimo Dog Type): Autoimmune thrombocytopenia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Spitz thrombopathia, Thrombocytopathy, Thrombocytopenia
Thrombopathia (Basset Hound Type): Autoimmune thrombocytopenia, Basset Hound thrombopathia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Thrombocytopathy, Thrombocytopenia
Thrombopathia (Newfoundland Type): Autoimmune thrombocytopenia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Thrombocytopathy, Thrombocytopenia
Trapped Neutrophil Syndrome: Cohen syndrome, TNS

U

Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 1)
Ullrich Congenital Muscular Dystrophy (Labrador Retriever Type 2)
Urolithiasis (Native American Indian Dog Type): 2, 8-DHA Urolithiasis, 8-Dihydroxyadenine Urolithiasis

V

Van Den Ende-Gupta Syndrome: Skeletal Dysplasia Syndrome, VDEGS
Von Willebrand Disease I: Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 1, von Willebrand's disease, VWDI
Von Willebrand Disease II: pseudohemophilia, vascular hemophilia, von Willebrand disease type 2, Von Willebrand's disease
Von Willebrand Disease III (Kooikerhondje Type): Pseudohemophilia, Vascular hemophilia, von Willebrand's disease, VWDIII
Von Willebrand Disease III (Scottish Terrier Type): Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 3, von Willebrand's disease, VWDIII
Von Willebrand Disease III (Shetland Sheepdog Type): Pseudohemophilia, Vascular hemophilia, von Willebrand's disease, VWDIII

Disease Test Catalog

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