Special order genetic tests for dogs
Genetic diseases
H627 Aberrant Autophagy (LSD)
H366 IGS (Selective Cobalamin Malabsorption) 1
H386 Achromatopsia 2 (cone degeneration, hemeralopia)
H367 IGS (Selective Cobalamin Malabsorption) 2
H387 Achromatopsia 3 (cone degeneration, hemeralopia)
H332 IGS (Selective Cobalamin Malabsorption) 3
H396 Adult Onset Neuropathy (AON)
H329 Juvenile Laryngeal Paralysis Polyneuropathy (JLPP)
H389 Alexander Disease
H724 L2-HGA
H351 Amelogenesis Imperfecta
H395 Limb girdle muscular dystrophy (LGMD) 1
H450 Bleeding disorder due to P2RY12 defect
H317 Macular Corneal Dystrophy
H487 Brachyury (Bobtail)
H746 Maligne Hyperthermia
H412 C3 Deficiency
H629 MDR1 (partner lab)
H749 Centronuclear Myopathy (CNM, also known as HMLR)
H427 MTM
H413 Cerebellar Abiotrophy (NCCD)
H451 Mucopolysaccharidose Type VII – 2
H410 Cerebellar Ataxia
H418 Mucopolysaccharidosis Type IIIa
H331 Cerebellar Ataxia (SDCA1)
H748 Mucopolysaccharidosis Type VII
H804 Cerebellar Ataxia / NCL-A
H306 Multifocal Retinopathy 3 (cmr3) 1
H653 Cerebellar Ataxia 2
H307 Multifocal Retinopathy 3 (cmr3) 2
H411 Cerebellar Ataxia, progressive early-onset
H747 Muscular Dystrophy (GRMD)
H318 Cerebellar Cortical Degeneration
H359 Muscular Dystrophy, Duchenne Type (DMD)
H355 Cerebellar Hypoplasia Resembling
H419 Muscular Dystrophy, Duchenne type (MDM)
H356 Chondrodysplasia, Disproportionate Short-Limbed
H493 Muscular hypertrophy (double muscling)
H709 CLAD, Type I
H424 Musladin-Lueke syndrome (MLS)
H484 CLAD, Type III
H391 Myasthenia gravis-like disease
H871 CMR1 (Canine Multifocal Retinopathy)
H368 Myopathy
H730 CMR2 (Canine Multifocal Retinopathy)
H738 Myotonia Congenita
H630 Coat Colour Merle (partner lab)
H498 Myotonia Congenita 2
H705 Collie Eye Anomaly (CEA_CH, partnerlab)
H707 Narcolepsy 1
H710 Collie Eye Anomaly (CEA_CH, patent owner Optigen)
H697 Narcolepsy 2
H918 Cone Degeneration
H698 Narcolepsy 3
H357 Cone Rod Dystrophy 1 (crd1)
H812 Neonatal Encephalopathy
H358 Cone Rod Dystrophy 2 (crd2)
H370 Nephritis
H625 Congenital Cornification Disorder
H428 Neuroaxonal Dystrophy
H416 Congenital Hypothyroidism (CHG) 1
H494 Neuronal ceroid lipofuscinosis (NCL) 1
H485 Congenital Hypothyroidism (CHG) 2
H429 Neuronal ceroid lipofuscinosis (NCL) 10
H488 Congenital Hypothyroidism (CHG) 3
H499 Neuronal ceroid lipofuscinosis (NCL) 2
H425 Congenital Myasthenic Syndrome
H721 Neuronal ceroid lipofuscinosis (NCL) 5
H626 Congenital Myasthenic Syndrome 2
H380 Neuronal ceroid lipofuscinosis (NCL) 5 GR
H701 Coppertoxicosis
H330 Neuronal ceroid lipofuscinosis (NCL) 6
H312 Craniomandibular Osteopathy (CMO)
H652 Neuronal ceroid lipofuscinosis (NCL) 8
H856 crd3
H393 Oculocutaneous Albinism
H766 crd4-PRA (previously cord1-PRA)
H430 Osteogenesis imperfecta
H728 CSNB (Congenital Stationary Night Blindness)
H431 Osteogenesis imperfecta 2
H703 Cystinuria I – A – 1
H381 Osteogenesis Imperfecta 3
H644 Cystinuria, type II – A
H305 PAP-PRA1 1
H643 Cystinuria, type II – A – 1
H301 PAP-PRA1 2
H645 Cystinuria, type II – B
H717 PFK (Phosphofructokinase Deficiency)
H308 Degenerative Myelopathy 2 (DM2 Bernese mountain)
H872 Pituitary dwarfism
H673 Degenerative Myelopathy, DM (partner lab)
H509 Polycystic kidney disease (PKD1)
H806 Degenerative Myelopathy, DM (patent owner)
H438 Polycythemia
H327 Dental Hypomineralization (Raine Syndrome)
H914 Polyneuropathy 1
H489 Dermatofibrosis
H495 Polyneuropathy 2
H434 Dilated Cardiomyopathy (DCM)
H379 Polyneuropathy 3 (LPN1)
H375 Dog_Skin Fragility
H371 PRA
H377 Dog_Spinal Dysraphism
H390 PRA 2
H739 Dominant PRA
H394 PRA BBS4
H913 Dry Eye Curly Coat Syndrome
H372 PRA crdPRA
H385 Ectodermal Dysplasia X-linked
H382 PRA erd
H497 Epidermolysis bullosa, dystrophic (RDEB)
H373 PRA type 3
H486 Epilepsy, BFJ
H704 prcd PRA (partnerlab)
H674 Episodic Falling Disease (partner lab)
H700 prcd PRA (patent owner Optigen)
H883 Episodic Falling Disease (patent owner)
H439 Prekallikrein deficiency
H672 Exercise Induced Collapse, EIC (partner lab)
H414 Primary Ciliary dyskinesia
H805 Exercise Induced Collapse, EIC (patent owner)
H383 Primary Glaucoma
H607 Factor IX Deficiency
H374 Primary Hyperoxaluria
H435 Factor VII deficiency
H849 Primary Lens Luxation (PLL)
H324 FBN2
H740 Pyruvate Dehydrogenase Phosphatase 1 (PDP1)
H676 FN, Familial Nephropathy (partner lab)
H741 Pyruvate kinase Deficiency (PKDef)
H729 FN, Familial Nephropathy (patent owner)
H454 Pyruvatekinase Deficiency (PKDef) 2
H736 Fucosidosis
H455 Pyruvatekinase Deficiency (PKDef) 3
H360 Gallbladder Mucocele
H768 rcd1 PRA
H361 Gangliosidosis, GM2, Type I (B variant)
H769 rcd1a PRA
H490 Gangliosidosis, GM2, type II
H801 rcd2 PRA
H496 Glaucoma (POAG)
H770 rcd3 PRA
H737 Globoid Cell Leukodystrophy / Krabbes Disease
H511 rcd4 PRA
H415 Glycogen Storage Disease GSD I
H794 Retinal Dysplasia Retinal Folds RD OSD 1
H813 Glycogen Storage Disease GSD Type IIIa (GSDIIIa)
H426 Retinal Dysplasia Retinal Folds RD OSD 2
H702 GM1
H423 SCID
H915 gPRA
H456 SCID 2
H868 GR_PRA1
H388 Sensory Neuropathy
H473 GR_PRA2
H510 Skeletal Dysplasia 2 (SD2)
H752 Gray Collie Syndrome (Cyclic Neutropenia)
H303 Spinocerebellar ataxia
H491 Haemophilia A (Factor VIII) (partner lab)
H328 Spinocerebellar ataxia (2)
H436 Haemophilia A (Factor VIII) (patent owner)
H440 Thrombasthenia
H392 Hemorragic diathesis (Scott Syndrome)
H447 Thrombasthenia 2
H809 Hereditary Cataract (HC) – HSF4
H441 Thrombocytopaenia
H699 Hereditary Cataract 2 (HSF4)
H442 Thrombopathia
H919 Hiplaxity 1
H448 Thrombopathia 2
H421 Hiplaxity 2
H449 Thrombopathia 3
H675 HNPK (partner lab)
H787 Trapped Neutrophil Syndrome (TNS)
H443 HNPK (patent owner)
H432 Tremor, X-linked
H363 Hyperkeratosis, epidermolytic
H771 Type A PRA
H492 Hyperkeratosis, palmoplantar
H433 Vitamin D-deficiency rickets, type II
H811 Hyperuricemia (HUU)
H642 Von Willebrand disease 3 – 2
H364 Hypocatalasia
H677 Von-Willebrands Disease Type 1
H365 Hypomyelination
H743 Von-Willebrands Disease Type 2
H873 Ichthyosis 2
H744 Von-Willebrands Disease Type 3
H304 Ichthyosis 3
H696 Warburg Micro Syndrome 1 (WARBM1)
H378 Ichthyosis 4
H772 X Linked PRA1 (XL PRA1)
H384 Ichthyosis 5
H745 X-SCID
Other genetic traits
H820 Coat Colour A-locus
H930 Coat Colour Merle (patent owner)
H733 Coat Colour B-locus
H354 Coat Colour Panda White Spotting
H847 Coat Colour D-Locus Improved (MLPH)
H326 Coat Colour Piebald
H734 Coat Colour E-locus
H353 Coat Colour Saddle tan vs black-and-tan
H818 Coat Colour Em-locus
H921 Curly Coat
H316 Coat Colour H-locus (Harlequin)
H765 Hair length
H819 Coat Colour K-locus
H848 Improper Coat/Furnishings

All of the dogs or images featured on this page belong to Weatherbys staff. A big thank you to Hannah Slough, Adrian Howes, Ellie Everitt, Kim Christer, Imam Uddin, Suzanne Barnes, Caroline Bray, Abbey Cochrane, Jamie Clark, Jadelouise York, Sharon Newick, Clare Lewis, Ben Roe, Allyce Hollender, Lindsey Tibbetts, Jenny McLaren, Denise Schmitz, Chris Bennett and all the dogs for being very good boys and girls.