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

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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.