Health Conditions List

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID

Multisystem FAM83H Exon 5

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency

Multisystem PFKM, Whippet and English Springer Spaniel Variant

Glycogen storage disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency

Multisystem PFKM, Wachtelhund Variant

Lagotto Storage Disease

Multisystem ATG4D

Neuronal Ceroid Lipofuscinosis 1, NCL 1

Multisystem PPT1 Exon 8, Dachshund Variant 1

Neuronal Ceroid Lipofuscinosis 2, NCL 2

Multisystem TPP1 Exon 4, Dachshund Variant 2

Neuronal Ceroid Lipofuscinosis, Cerebellar Ataxia, NCL4A

Multisystem ARSG Exon 2, American Staffordshire Terrier Variant

Neuronal Ceroid Lipofuscinosis 5, NCL 5

Multisystem CLN5 Exon 4 SNP, Border Collie Variant

Neuronal Ceroid Lipofuscinosis 6, NCL 6

Multisystem CLN6 Exon 7, Australian Shepherd Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8

Multisystem CLN8 Exon 2, English Setter Variant

Neuronal Ceroid Lipofuscinosis 7, NCL 7

Multisystem MFSD8, Chihuahua and Chinese Crested Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8

Multisystem CLN8, Australian Shepherd Variant

Neuronal Ceroid Lipofuscinosis 10, NCL 10

Multisystem CTSD Exon 5, American Bulldog Variant

Neuronal Ceroid Lipofuscinosis 5, NCL 5

Multisystem CLN5 Exon 4 Deletion, Golden Retriever Variant

Late-Onset Neuronal Ceroid Lipofuscinosis, NCL 12

Multisystem ATP13A2, Australian Cattle Dog Variant

GM1 Gangliosidosis

Multisystem GLB1 Exon 15, Shiba Inu Variant

GM1 Gangliosidosis

Multisystem GLB1 Exon 15, Alaskan Husky Variant

GM1 Gangliosidosis

Multisystem GLB1 Exon 2, Portuguese Water Dog Variant

GM2 Gangliosidosis

Multisystem HEXB, Poodle Variant

GM2 Gangliosidosis

Multisystem HEXA, Japanese Chin Variant

Globoid Cell Leukodystrophy, Krabbe disease

Multisystem GALC Exon 5, Terrier Variant

Neuronal Ceroid Lipofuscinosis 8, NCL 8

Multisystem CLN8 Insertion, Saluki Variant

Mucopolysaccharidosis IIIB, Sanfilippo Syndrome Type B, MPS IIIB

Multisystem NAGLU, Schipperke Variant

Primary Ciliary Dyskinesia, PCD

Multisystem STK36, Australian Shepherd Variant

Congenital Dyserythropoietic Anemia and Polymyopathy

Multisystem EHPB1L1, Labrador Retriever Variant

Glycogen Storage Disease Type IA, Von Gierke Disease, GSD IA

Multisystem G6PC1, German Pinscher Variant

Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia

Other Systems ENAM Deletion, Italian Greyhound Variant

Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia

Other Systems ENAM SNP, Parson Russell Terrier Variant

Persistent Mullerian Duct Syndrome, PMDS

Other Systems AMHR2

Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS

Other Systems MYO7A

Unilateral Deafness and Vestibular Syndrome

Other Systems PTPRQ Exon 39, Doberman Pinscher

Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever

Other Systems MTBP

Neonatal Interstitial Lung Disease

Other Systems LAMP3

Recurrent Inflammatory Pulmonary Disease, RIPD

Other Systems AKNA, Rough Collie Variant

Early Onset Adult Deafness, EOAD

Other Systems EPS8L2 Deletion, Rhodesian Ridgeback Variant

Early Bilateral Deafness

Other Systems LOXHD1 Exon 38, Rottweiler Variant

Alaskan Husky Encephalopathy, Subacute Necrotizing Encephalomyelopathy

Brain and Spinal Cord SLC19A3

Alexander Disease

Brain and Spinal Cord GFAP

Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration, NCCD

Brain and Spinal Cord SPTBN2, Beagle Variant

Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia

Brain and Spinal Cord SEL1L, Finnish Hound Variant

Cerebellar Hypoplasia

Brain and Spinal Cord VLDLR, Eurasier Variant

Spinocerebellar Ataxia, Late-Onset Ataxia, LoSCA

Brain and Spinal Cord CAPN1

Spinocerebellar Ataxia with Myokymia and/or Seizures

Brain and Spinal Cord KCNJ10

Hereditary Ataxia, Cerebellar Degeneration

Brain and Spinal Cord RAB24, Old English Sheepdog and Gordon Setter Variant

Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy

Brain and Spinal Cord LGI2

Degenerative Myelopathy, DM

Brain and Spinal Cord SOD1A

Fetal-Onset Neonatal Neuroaxonal Dystrophy

Brain and Spinal Cord MFN2, Giant Schnauzer Variant

Hypomyelination and Tremors

Brain and Spinal Cord FNIP2, Weimaraner Variant

Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome

Brain and Spinal Cord PLP1, English Springer Spaniel Variant

L-2-Hydroxyglutaricaciduria, L2HGA

Brain and Spinal Cord L2HGDH, Staffordshire Bull Terrier Variant

Neonatal Encephalopathy with Seizures, NEWS

Brain and Spinal Cord ATF2

Alaskan Malamute Polyneuropathy, AMPN

Brain and Spinal Cord NDRG1 SNP

Narcolepsy

Brain and Spinal Cord HCRTR2 Intron 4, Doberman Pinscher Variant

Narcolepsy

Brain and Spinal Cord HCRTR2 Intron 6, Labrador Retriever Variant

Narcolepsy

Brain and Spinal Cord HCRTR2 Exon 1, Dachshund Variant

Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD

Brain and Spinal Cord SERAC1 Exon 15, Kerry Blue Terrier Variant

Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration, CMSD

Brain and Spinal Cord SERAC1 Exon 4, Chinese Crested Variant

Juvenile Laryngeal Paralysis and Polyneuropathy, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, POANV

Brain and Spinal Cord RAB3GAP1, Rottweiler Variant

Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome, AMS

Brain and Spinal Cord GDNF-AS, Spaniel and Pointer Variant

Sensory Neuropathy

Brain and Spinal Cord FAM134B, Border Collie Variant

Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 1, LPN1

Brain and Spinal Cord LPN1, ARHGEF10

Juvenile Myoclonic Epilepsy

Brain and Spinal Cord DIRAS1

Juvenile-Onset Polyneuropathy, Leonberger Polyneuropathy 2, LPN2

Brain and Spinal Cord GJA9

Spongy Degeneration with Cerebellar Ataxia 1, SDCA1, SeSAME/EAST Syndrome

Brain and Spinal Cord KCNJ10

Spongy Degeneration with Cerebellar Ataxia 2, SDCA2

Brain and Spinal Cord ATP1B2

Neuroaxonal Dystrophy, NAD

Brain and Spinal Cord TECPR2, Spanish Water Dog Variant

Neuroaxonal Dystrophy, NAD

Brain and Spinal Cord VPS11, Rottweiler Variant

Exercise-Induced Collapse, EIC

Brain and Spinal Cord DNM1

Leukodystrophy

Brain and Spinal Cord TSEN54 Exon 5, Standard Schnauzer Variant

Spinocerebellar Ataxia

Brain and Spinal Cord SCN8A, Alpine Dachsbracke Variant

Hereditary Ataxia

Brain and Spinal Cord PNPLA8, Australian Shepherd Variant

Hereditary Cerebellar Ataxia

Brain and Spinal Cord SELENOP, Belgian Shepherd Variant

Dilated Cardiomyopathy, DCM1

Heart PDK4, Doberman Pinscher Variant 1

Dilated Cardiomyopathy, DCM2

Heart TTN, Doberman Pinscher Variant 2

Long QT Syndrome

Heart KCNQ1

Cardiomyopathy and Juvenile Mortality

Heart YARS2

Dilated Cardiomyopathy, DCM

Heart RBM20, Schnauzer Variant

Muscular Dystrophy

Muscular DMD, Cavalier King Charles Spaniel Variant 1

Muscular Dystrophy

Muscular DMD, Golden Retriever Variant

Limb Girdle Muscular Dystrophy

Muscular SGCD, Boston Terrier Variant

Ullrich-like Congenital Muscular Dystrophy

Muscular COL6A3 Exon 10, Labrador Retriever Variant

Centronuclear Myopathy, CNM

Muscular PTPLA

Inherited Myopathy of Great Danes

Muscular BIN1

Myostatin Deficiency, Bully Whippet Syndrome

Muscular MSTN

Myotonia Congenita

Muscular CLCN1 Exon 7, Miniature Schnauzer Variant

Myotonia Congenita

Muscular CLCN1 Exon 23, Australian Cattle Dog Variant

Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM

Muscular MTM1, Labrador Retriever Variant

Inflammatory Myopathy

Muscular SLC25A12

Nemaline Myopathy

Muscular NEB, American Bulldog Variant

Ullrich-like Congenital Muscular Dystrophy

Muscular COL6A1 Exon 3, Landseer Variant

Limb-Girdle Muscular Dystrophy 2D

Muscular SGCA Exon 3, Miniature Dachshund Variant

Myotonia Congenita

Muscular CLCN1 Exon 19, Labrador Retriever Variant

Muscular Dystrophy-Dystroglycanopathy

Muscular LARGE1, Labrador Retriever Variant

Congenital Muscular Dystrophy

Muscular LAMA2, Italian Greyhound

Hypocatalasia, Acatalasemia

Metabolic CAT

Pyruvate Dehydrogenase Deficiency

Metabolic PDP1, Spaniel Variant

Malignant Hyperthermia

Metabolic RYR1

Mucopolysaccharidosis Type VI, Maroteaux-Lamy Syndrome, MPS VI

Metabolic ARSB Exon 5, Miniature Pinscher Variant

Succinic Semialdehyde Dehydrogenase Deficiency

Metabolic ALDH5A1 Exon 7, Saluki Variant

β-Mannosidosis

Metabolic MANBA Exon 16, Mixed-Breed Variant

Medium-Chain Acyl-CoA Dehydrogenase Deficiency, MCADD

Metabolic ACADM, Cavalier King Charles Spaniel Variant

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption

Gastrointestinal CUBN Exon 53, Border Collie Variant

Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption

Gastrointestinal CUBN Exon 8, Beagle Variant

Inherited Selected Cobalamin Malabsorption with Proteinuria

Gastrointestinal CUBN, Komondor Variant

Lundehund Syndrome

Gastrointestinal LEPREL1

Intestinal Lipid Malabsorption

Gastrointestinal ACSL5, Australian Kelpie

Copper Toxicosis (Accumulating)

Liver ATP7B

Congenital Myasthenic Syndrome, CMS

Neuromuscular CHAT, Old Danish Pointing Dog Variant

Congenital Myasthenic Syndrome, CMS

Neuromuscular COLQ, Labrador Retriever Variant

Congenital Myasthenic Syndrome, CMS

Neuromuscular CHRNE, Jack Russell Terrier Variant

Congenital Myasthenic Syndrome, CMS

Neuromuscular COLQ, Golden Retriever Variant

Myasthenia Gravis-Like Syndrome

Neuromuscular CHRNE, Heideterrier Variant

Episodic Falling Syndrome

Neuromuscular BCAN

Paroxysmal Dyskinesia, PxD

Neuromuscular PIGN

Demyelinating Polyneuropathy

Neuromuscular SBF2/MTRM13

Laryngeal Paralysis

Neuromuscular RAPGEF6, Miniature Bull Terrier Variant

Laryngeal Paralysis and Polyneuropathy

Neuromuscular CNTNAP1, Leonberger, Saint Bernard, and Labrador Retriever variant

Dystrophic Epidermolysis Bullosa

Skin & Connective Tissues COL7A1, Golden Retriever Variant

Dystrophic Epidermolysis Bullosa

Skin & Connective Tissues COL7A1, Central Asian Shepherd Dog Variant

Ectodermal Dysplasia, Skin Fragility Syndrome

Skin & Connective Tissues PKP1, Chesapeake Bay Retriever Variant

Ichthyosis, Epidermolytic Hyperkeratosis

Skin & Connective Tissues KRT10, Terrier Variant

Ichthyosis, ICH1

Skin & Connective Tissues PNPLA1, Golden Retriever Variant

Ichthyosis

Skin & Connective Tissues SLC27A4, Great Dane Variant

Ichthyosis

Skin & Connective Tissues NIPAL4, American Bulldog Variant

Ichthyosis

Skin & Connective Tissues ASPRV1 Exon 2, German Shepherd Variant

Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita

Skin & Connective Tissues KRT16, Dogue de Bordeaux Variant

Hereditary Footpad Hyperkeratosis

Skin & Connective Tissues FAM83G, Terrier and Kromfohrlander Variant

Hereditary Footpad Hyperkeratosis

Skin & Connective Tissues DSG1, Rottweiler Variant

Hereditary Nasal Parakeratosis, HNPK

Skin & Connective Tissues SUV39H2

Musladin-Lueke Syndrome, MLS

Skin & Connective Tissues ADAMTSL2

Oculocutaneous Albinism, OCA

Skin & Connective Tissues SLC45A2, Small Breed Variant

Bald Thigh Syndrome

Skin & Connective Tissues IGFBP5

Lethal Acrodermatitis, LAD

Skin & Connective Tissues MKLN1

Ehlers Danlos

Skin & Connective Tissues ADAMTS2, Doberman Pinscher Variant

Oculocutaneous Albinism, OCA

Skin & Connective Tissues SLC45A2 Exon 6, Bullmastiff Variant

Junctional Epidermolysis Bullosa

Skin & Connective Tissues LAMB3 Exon 11, Australian Shepherd Variant

Hereditary Nasal Parakeratosis

Skin & Connective Tissues SUV39H2 Intron 4, Greyhound Variant

Junctional Epidermolysis Bullosa

Skin & Connective Tissues LAMA3 Exon 66, Australian Cattle Dog Variant

Congenital Cornification Disorder

Skin & Connective Tissues NSDHL, Chihuahua Variant

Ehlers-Danlos Syndrome (EDS)

Skin & Connective Tissues COL5A1, Labrador Retriever Variant

Ichthyosis, ICH2

Skin & Connective Tissues ABHD5, Golden Retriever Variant

Darier Disease

Skin & Connective Tissues ATP2A2, Irish Terrier Variant

Cleft Lip and/or Cleft Palate

Skeletal ADAMTS20, Nova Scotia Duck Tolling Retriever Variant

Hereditary Vitamin D-Resistant Rickets

Skeletal VDR

Oculoskeletal Dysplasia 2, Dwarfism-Retinal Dysplasia 2, drd2, OSD2

Skeletal COL9A2, Samoyed Variant

Osteogenesis Imperfecta, Brittle Bone Disease

Skeletal COL1A2, Beagle Variant

Osteogenesis Imperfecta, Brittle Bone Disease

Skeletal SERPINH1, Dachshund Variant

Osteogenesis Imperfecta, Brittle Bone Disease

Skeletal COL1A1, Golden Retriever Variant

Osteochondrodysplasia, Skeletal Dwarfism

Skeletal SLC13A1, Poodle Variant

Skeletal Dysplasia 2, SD2

Skeletal COL11A2, Labrador Retriever Variant

Craniomandibular Osteopathy, CMO

Skeletal SLC37A2

Raine Syndrome, Canine Dental Hypomineralization Syndrome

Skeletal FAM20C

Chondrodystrophy and Intervertebral Disc Disease, CDDY/IVDD, Type I IVDD

Skeletal FGF4 retrogene - CFA12

Chondrodysplasia

Skeletal ITGA10, Norwegian Elkhound and Karelian Bear Dog Variant

Hypophosphatasia

Skeletal ALPL Exon 9, Karelian Bear Dog Variant

Disproportionate Dwarfism

Skeletal PRKG2, Dogo Argentino Variant

Craniomandibular Osteopathy, CMO

Skeletal SLC37A2 Intron 16, Basset Hound Variant

Cleft Palate, CP1

Skeletal DLX6 intron 2, Nova Scotia Duck Tolling Retriever Variant

Dental-Skeletal-Retinal Anomaly

Skeletal MIA3, Cane Corso Variant

Browse all health conditions

MDR1 Drug Sensitivity

Alanine Aminotransferase Activity

Copper Toxicosis (Attenuating)

Copper Toxicosis (Attenuating)

P2Y12 Receptor Platelet Disorder

Factor IX Deficiency, Hemophilia B

Factor IX Deficiency, Hemophilia B

Factor VII Deficiency

Factor VIII Deficiency, Hemophilia A

Factor VIII Deficiency, Hemophilia A

Factor VIII Deficiency, Hemophilia A

Thrombopathia

Thrombopathia

Thrombopathia

Von Willebrand Disease Type III, Type III vWD

Von Willebrand Disease Type III, Type III vWD

Von Willebrand Disease Type I, Type I vWD

Von Willebrand Disease Type III, Type III vWD

Von Willebrand Disease Type II, Type II vWD

Factor XI Deficiency

Canine Leukocyte Adhesion Deficiency Type I, CLAD I

Canine Leukocyte Adhesion Deficiency Type III, CLAD III

Canine Elliptocytosis

Glanzmann's Thrombasthenia Type I

Glanzmann's Thrombasthenia Type I

May-Hegglin Anomaly

Congenital Macrothrombocytopenia

Prekallikrein Deficiency

Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency

Trapped Neutrophil Syndrome, TNS

Ligneous Membranitis, LM

Platelet Factor X Receptor Deficiency, Scott Syndrome

Methemoglobinemia

Bernard-Soulier Syndrome, BSS

Methemoglobinemia

Congenital Hypothyroidism

Congenital Hypothyroidism with Goiter

Congenital Hypothyroidism

Congenital Dyshormonogenic Hypothyroidism with Goiter

Pituitary Dwarfism

Proportionate Dwarfism

Complement 3 Deficiency, C3 Deficiency

Severe Combined Immunodeficiency, SCID

Severe Combined Immunodeficiency, SCID

X-linked Severe Combined Immunodeficiency, X-SCID

X-linked Severe Combined Immunodeficiency, X-SCID

Progressive Retinal Atrophy, rcd1

Progressive Retinal Atrophy, rcd3

Progressive Retinal Atrophy, CNGA

Progressive Retinal Atrophy, prcd

Progressive Retinal Atrophy, PRA1

Progressive Retinal Atrophy

Golden Retriever Progressive Retinal Atrophy 1, GR-PRA1

Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2

Progressive Retinal Atrophy, crd1

Progressive Retinal Atrophy, crd4/cord1

X-Linked Progressive Retinal Atrophy 1, XL-PRA1

Progressive Retinal Atrophy, PRA3

Collie Eye Anomaly, Choroidal Hypoplasia, CEA

Day Blindness, Cone Degeneration, Achromatopsia

Achromatopsia

Achromatopsia

Autosomal Dominant Progressive Retinal Atrophy

Canine Multifocal Retinopathy, cmr1

Canine Multifocal Retinopathy, cmr2

Canine Multifocal Retinopathy, cmr3

Primary Open Angle Glaucoma

Primary Open Angle Glaucoma

Primary Open Angle Glaucoma

Primary Open Angle Glaucoma and Primary Lens Luxation

Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts

Primary Lens Luxation

Congenital Stationary Night Blindness

Congenital Stationary Night Blindness

Macular Corneal Dystrophy, MCD