Health Tested

Genetic Health Conditions we test 

OFA  HIPS and ELBOWS

ACVO OFA EYE (CAER)

PRCD PROGRESSIVE RETINAL ATROPHY 

FULL DENTITION - NORMAL

PATELLA - NORMAL

Blood Clearances:

P2y12 Receptor Platelet Disorder

Factor IX Deficiency, Hemophilia B - F9 Exon 7 

Factor VIII Deficiency Hemophilia A - F8 Exon 11  

Factor VIII Deficiency Hemophilia A - F8 Exon 1 

Copper Toxicosis (Attenuating)  ATP7A and ATP7B 

Thrombopathia Exon 5 

Thrombopathia Exon 8 

Von Willebrand Disease Type III 

Von Willebrand Disease Type II 

Von Willebrand Disease Type I 

Canine Leukocyte Adhesion Deficiency Type III (LAD3) 

Congenital Macrothrombocytopenia 

Canine Elliptocytosis 

Canine Neutropenia 

Glanzmann's Thrombasthenia Type I - 

May-Hegglin Anomaly 

Prekallikrein Deficiency 

Pyruvate Kinase Deficiency Exon 5 

Pyruvate Kinase Deficiency Exon 7 

Pyruvate Kinase Deficiency Exon 10 

Trapped Neutrophil Syndrome 

Ligneous Membranitis 

Immune Clearances:

Complement 3 (C3) Deficiency 

Severe Combined Immunodeficiency - PRKDC 

Severe Combined Immunodeficiency - RAG1 

X-Linked Severe Combined Immunodeficiency - Variant 1 

X-Linked Severe Combined Immunodeficiency - Variant 2

Hormone Clearances:

Congenital Hypothyroidism

Eye Clearances:

Progressive Retinal Atrophy - PRCD1 

Progressive Retinal Atrophy - PRCD3 

Progressive Retinal Atrophy - CNGA 

Progressive Retinal Atrophy - PRCD 

Progressive Retinal Atrophy - CNGB1 

Progressive Retinal Atrophy - SAG 

Progressive Retinal Atrophy 1 - SLC4A3 

Progressive Retinal Atrophy 2 - TTC8 

Progressive Retinal Atrophy - CRD1 - PDE6B 

Progressive Retinal Atrophy - CRD2 - IQCB1 

Progressive Retinal Atrophy - CRD4/CORD1 - RPGRIP1 

Choroidal Hypoplasia - NHEJ1 

Achromatopsia - CNGA3 Exon 7 

Autosomal Dominant Progressive Retinal Atrophy 

Canine Multifocal Retinopathy - CMR1 

Canine Multifocal Retinopathy - CMR3 

Stargardt Disease (ABCA4 Exon 28, Labrador Retriever Variant)

Canine Multifocal Retinopathy - CMR3 - BEST1 EXON 10 SNP 

Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 9 

Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 17 

Glaucoma - Primary Open Angle Glaucoma - ADAMTS17 Exon 11

Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 2 

Hereditary Cataracts, Early Onset Cataracts, Juvenile Cataracts 

Primary Lens Luxation 

Congenital Stationary Night Blindness 

Macular Corneal Dystrophy (MCD) 

Clinical Clearances:

MDR1 Drug Sensitivity

Alanine Aminotransfearase (ALT) Activity 

MULTISYSTEM CLEARANCES:

Glycogen Storage Disease Von Gierke Disease 

Primary Ciliary Dyskinesia 

Congenital Keratoconjunctivitis Sicca & Ichthyosiform Dermatosis (CKCSID)

Dry Eye Curly Coat Syndrome 

X-Linked Ectodermal Dysplasia

Anhidrotic Ectodermal Dysplasia

Renal Cystadenocarcinoma & Nodular Dermatofibrosis (RCND)

Canine Fucosidosis 

Glycogen Storage Disease Type II Pompe's Disease 

Glycogen Storage Disease Type IIIa (GSD IIIa) 

Mucopolysaccharidosis Type I 

Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 1

Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 2 

Mucopolysaccharidosis Type VII Exon 3 Sly Syndrome 

Mucopolysaccharidosis Type VII Exon 5 Sly

Syndrome 

Glycogen Storage Disease Type II Phosphofructokinase Deficiency

Lagotto Storage Disease 

Neuronal Ceroid Lipofuscinosis 1 

Neuronal Ceroid Lipofuscinosis 2 

Neuronal Ceroid Lipofuscinosis 1 - Cerebellar Ataxia NCL A

Neuronal Ceroid Lipofuscinosis 1 - CLN5 

Neuronal Ceroid Lipofuscinosis 6 - CLN6 Exon 7

Neuronal Ceroid Lipofuscinosis 8 - CLN8 

Neuronal Ceroid Lipofuscinosis 

Neuronal Ceroid Lipofuscinosis 10 - CTSD Exon 5 

Adult Onset Neuronal Ceroid Lipofuscinosis 

GM1 Gangliosidosis Exon 2 

GM1 Gangliosidosis Exon 15

GM2 Gangliosidosis Exon 2

GM2 Gangliosidosis Hexa 

Globoid Cell Leukodystrophy, Krabbe Disease 

BRAIN & SPINAL CORD CLEARANCES:

Alexander Disease 

Encephalopathy, Subacute Necrotizing Encephalomyelopathy 

Cerebellar Abiotrophic, Neonatal Cerebellar Cortical Degeneration 

Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia 

Cerebellar Hypoplasia 

Spinocerebellar Ataxia, Late-Onset Ataxia 

Spinocerebellar Ataxia with Myokymia and/or Seizures

Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy

Degenerative Myelopathy

Fetal-Onset Neonatal Neuroaxonal Dystrophy 

Hypomyelination & Tremors 

Shaking Puppy Syndrome, X-Linked Generalized Tremor Syndrome 

L-2-Hydroxyglutaric Aciduria

Neonatal Encephalopathy with Seizures (NEWS) 

Polyneuropathy, NDRG1 Exon 15 

Polyneuropathy, NDRG1 Exon 4

Narcolepsy 

Progressive Neuronal Abiotrophic (canine Multiple System Degeneration) Exon 4

Progressive Neuronal Abiotrophic (canine Multiple System Degeneration) Exon 15

Juvenile Laryngeal Paralysis & Polyneuropathy, Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV)

Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome

Juvenile Onset Polyneuropathy, Leonberger Polyneuropathy 1

Spongy Degeneration with Cerebellar Ataxia 1, SeSAME/EAST

Spongy Degeneration with Cerebellar Ataxia 2, SeSAME/EAST 

SKELETAL CLEARANCES:

Cleft Lip and/or Cleft Palate

Hereditary Vitamin D-Resistant Rickets 

Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia 

Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) 

Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) 

Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1) 

Osteochondrodysplasic, Skeletal Dwarfism 

Skeletal Dysplasia 2 

Craniomandibular Osteopathy (CMO) 

COAT COLOR CLEARANCES:

E Locus (MC1R) - No dark hairs

D Locus (MLPH) Does not carry Dilute 

B Locus (TYRP1) Produces Black pigment in skin, noses, eye rims and footpads