| Article nr. |
Description |
More info |
| H810 | Sensory Ataxic Neuropathy (SAN) |  |
| H804 | Cerebellar Ataxia |  |
| H721 | CL (Neuronal Ceroid Lipofuscinosis) |  |
| H709 | CLAD |  |
| H730 | CMR2 (Canine Multifocal Retinopathy) |  |
| H820 | Coat Colour A-locus |  |
| H733 | Coat Colour B-locus |  |
| H815 | Coat Colour D-locus |  |
| H734 | Coat Colour E-locus |  |
| H818 | Coat Colour Em-locus |  |
| H819 | Coat Colour K-locus |  |
| H710 | Collie Eye Anomaly Choroidal Hypoplasia (CEA_CH) |  |
| H701 | Coppertoxicosis |  |
| H766 | cord1-PRA |  |
| H856 | crd3 |  |
| H728 | CSNB (Congenital Stationary Night Blindness) |  |
| H703 | Cystenuria |  |
| H806 | Degenerative Myelopathy (DM) |  |
| H739 | Dominant PRA |  |
| H805 | Exercise Induced Collapse (EIC) |  |
| H729 | FN (Familial Nephropathy |  |
| H736 | Fucosidosis |  |
| H737 | Globoid Cell Leukodystrophy / Krabbes Disease |  |
| H813 | Glycogen Storage Disease GSD Type IIIa (GSDIIIa) |  |
| H702 | GM1 |  |
| H752 | Gray Collie Syndrome |  |
| H765 | Hair length |  |
| H809 | Hereditary Cataract (HC) |  |
| H811 | Hyperuricemia (HUU) |  |
| H848 | Improper Coat (IC13) |  |
| H731 | JDCM |  |
| H724 | L2-HGA |  |
| H746 | Maligne Hyperthermia |  |
| H723 | MDR1 |  |
| H748 | Mucopolysaccharidosis Type VII |  |
| H747 | Muscular Dystrophy (GRMD) |  |
| H749 | Myopathy (HMLR) |  |
| H738 | Myotonia Congenita |  |
| H707 | Narcolepsy |  |
| H812 | Neonatal Encephalopathy |  |
| H219 | Parentage Verfication Fox |  |
| H200 | Parentage Verification Dog |  |
| H717 | PFK (Phosphofructokinase Deficiency) |  |
| H700 | prcd PRA |  |
| H849 | Primary Lens Luxation (PLL) |  |
| H741 | Pyruvaatkinase Deficiency (PKDef) |  |
| H740 | Pyruvate Dehydrogenase Phosphatase 1 (PDP1) |  |
| H768 | rcd1 PRA |  |
| H769 | rcd1a PRA |  |
| H801 | rcd2 PRA |  |
| H770 | rcd3 PRA |  |
| H794 | Retinal Dysplasia Retinal Folds RD OSD |  |
| H302 | Sex Determination Hyena |  |
| H787 | Trapped Neutrophil Syndrome (TNS) |  |
| H771 | Type A PRA |  |
| H817 | Vitamin B12 (Intestinal Cobalamin) Deficiency |  |
| H742 | Von-Willebrands Disease Type 1 |  |
| H743 | Von-Willebrands Disease Type 2 |  |
| H744 | Von-Willebrands Disease Type 3 |  |
| H772 | X Linked PRA (XL PRA) |  |
| H745 | X-SCID |  |