(compreso di DEPOSITO e IVA) Hyperuricosuria (SLC) 60,0 Malignant hyperthermia (MH) 60,0 Degenerative myelopathy exon 2 (DM exon2 60,0 Acatalasemia

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1 Hyperuricosuria (SLC) 60,0 Malignant hyperthermia (MH) 60,0 Degenerative myelopathy exon 2 (DM exon2 60,0 Acatalasemia 60,0 Achromatopsia (day blindness) (ACHM-1) 60,0 Adult onset neuropathy (AON) 80,0 Akutes Lungenversagen (ARDS) 60,0 Alaskan Husky enzephalopathy (AHE) 60,0 Alaskan Malamute polyneuropathy (AMPN) 60,0 Amelogenesis imperfecta (AI) 60,0 Alexander disease 60,0 Bardet-Biedl syndrome (BBS) 60,0 Brachyuria (stumpy tail) 60,0 C-Lokus (albino) 60,0 C3 deficiency (C3) 60,0 Canine leucocyte adhesion deficiency (CLAD) 60,0 Canine multi-focal retinopathy (CMR1/2/3) 80,0 Canine Multiple System Degeneration (CMSD) 60,0 Cerebral dysfunction (CDFS) 60,0 Chondrodysplasia (dwarfism) 60,0 Cleft lip/palate and syndactyly (CLPS) 60,0 Collie eye anomaly (CEA) Optigen 160,0 Collie eye anomaly (CEA) partnerlaboratory 60,0 Combi: Ataxia (LOA + SCA) 90,0 Combi: Ataxia + PLL (LOA + SCA + PLL) 110,0 Combi: DM exon 2 + MDR1 100,0 Combi: Dry Eye Curly Coat + Episodic Falling 65,0 Combi: JE + LSD + Furnishing 110,0 Cone degeneration (CD) Optigen 170,0 Congenital hypothyroidism with goiter (CHG) 60,0 Congenital ichtyosis 60,0 Congenital myasthenic syndrome (CMS) 60,0 Congenital stationary night blindness (CSNB) 60,0 Copper toxicosis (CT) 60,0 Craniomandibular osteopathy (CMO) 60,0 Cystinuria 60,0

2 Dwarfism (pituitary form) 60,0 Dwarfism (Skeletal dysplasia 2)(SD2) 60,0 Dystrophic Epidermolysis bullosa (DEB) 60,0 Ectodermal dysplasia/skin fragility syndrome 60,0 Epidermolytic hyperkeratosis (EHK) 60,0 Episodic falling (EF) 60,0 Exercise induced collapse (EIC) 80,0 Factor VII deficiency 60,0 Familial nephropathy (FN) 60,0 Familial Nephropathy (FN) partnerlaboratory 80,0 Fanconi syndrome 60,0 Finnish Hound ataxia (FHA) 60,0 Fucosidosis 60,0 Gallbladder mucoceles 60,0 Glanzmann thrombasthenia (GT) 60,0 Globoid cell leucodystrophy (Krabbe-disease) 60,0 Glycogen sorage disease GSD Ia 60,0 Glycogen storage disease GSD II (Pompe) 60,0 Glycogen storage disease type IIIa (GSD3)a 60,0 GM1-Gangliosidosis (GM1) 60,0 GM2-gangliosidosis (Sandhoff disease) (GM2) 60,0 Grey Collie syndrome (GCS) 60,0 Hemophilia A (factor VIII deficiency) 80,0 Hemophilia B (factor IX deficiency) 80,0 Hemorragic diathesis (Scott syndrom) 60,0 Hereditary ataxia (HA) 60,0 Hereditary Cataract (HSF4) 60,0 Hereditary myopathy (CNM) 60,0 Hereditary nasal parakeratosis (HNPK) 60,0 Hereditary neuropathy (GHN) 60,0 Hereditäre nasale Parakeratose (HNPK) 110,0 Hypomyelination/Shaking puppy syndrome (SPS) 60,0 Ichthyosis 60,0 Imerslund-Gräsbeck syndrome (IGS) 60,0

3 Junctional epidermolysis bullosa (JEB) 60,0 Juvenile epilepsy (JE) 60,0 Juvenile laryngeal paralysis & polyneuropathy (JLPP) 60,0 Juvenile myoclonic epilepsy (JME) 60,0 L-2-hydroxyglutaric aciduria (L2HGA) 60,0 Lagotto storage disease (LSD) 60,0 Late onset ataxia (LOA) 60,0 Leonberger polyneuropathy (LPN1) 60,0 Leonberger Polyneuropathy 2 (LPN2) 60,0 Leukocyte adhesion deficiency type III (LAD3) 60,0 Lundehund syndrome 60,0 Macrothrombocytopenia (MTC) 60,0 May-Hegglin anomaly (MHA) 60,0 MDR1-gene defect(ivermectin hypersensibility) 60,0 Mucopolysaccharidosis type IIIa (MPS3a) 60,0 Mucopolysaccharidosis type VII (MPS 7) 60,0 Muscular dystrophy (MD) 60,0 Musladin-Lueke syndrome (MLS) 60,0 Myostation mutation ("bully"-gene) 60,0 Myotonia congenita 60,0 Narcolepsy 60,0 Necrotizing meningoencephalitis (NME/PDE) 60,0 Nemalin myopathy 60,0 Neonatal cortical cerebellar abiotrophy (NCCD 60,0 Neonatal encephalopathy with seizures (NEWS) 60,0 Neuroaxonal dystrophy (NAD) 60,0 Neuronal ceroid lipifuscinosis (NCL) 60,0 Neuronal ceroid lipifuscinosis (NCL) partnerlab 60,0 Obesity 60,0 Osteogenesis imperfecta (brittle bone dis.) 60,0

4 Paket Dobermann 130,0 Paket Landseer 130,0 Paket Rhodesian Ridgeback 130,0 Paket Rottweiler 130,0 Paroxysomal dyskinesia (PxD) 60,0 Persistent Müllerian duct snydrome (PMDS) 60,0 Phosphofructokinase deficiency (PFKD) 60,0 Polycystic kidney disease (PKD) 60,0 Postoperative hemorrhage (P2Y12) 60,0 Prekallikrein deficiency (KLK) 60,0 Primary ciliary dyskinesia (PCD) 60,0 Primary hyperoxaluria (PH) 60,0 Primary lens luxation (PLL) 60,0 Primary open angle glaucoma (POAG) 60,0 Primäres Weitwinkelglaukom u. Linsenluxation 60,0 Progressive retinal atrophia (crd2-pra) 60,0 Progressive retinal atrophia (rcd2-pra) 60,0 Progressive Retinal Atrophy (Bas_PRA) 60,0 Progressive retinal atrophy (CNGA1-PRA) 60,0 Progressive retinal atrophy (crd-pra) 60,0 Progressive retinal atrophy (g-pra) 60,0 Progressive retinal atrophy (GR_PRA1) 60,0 Progressive retinal atrophy (GR_PRA2) 60,0 Progressive Retinal Atrophy (pap_pra1) 60,0 Progressive retinal atrophy (PRA) 60,0 Progressive retinal atrophy (rcd4-pra) 60,0 Progressive retinal atrophy (XL-PRA) 60,0 Protein losing nephropathy (PLN) 60,0 Pyruvat dehydrogenase phosphatase 1deficiency 60,0 Pyruvate kinase deficiency (PK) 60,0 Raine syndrome 60,0 Renal Cystadenocarcinoma and nodular fibrosis 60,0 (RCND) Retinal dysplasia (OSD) Optigen 170,0 Retinal dysplasia (OSD) Partnerlaboratory 60,0 Sensorische Neuropathie (SN) 60,0 Severe combined immunodeficiency (SCID) 60,0 Shar Pei Autoinflammatory Disease (SPAID) 60,0

5 Renal Cystadenocarcinoma and nodular fibrosis (RCND) 60,0 Retinal dysplasia (OSD) Optigen 170,0 Retinal dysplasia (OSD) Partnerlaboratory 60,0 Sensorische Neuropathie (SN) 60,0 Severe combined immunodeficiency (SCID) 60,0 Shar Pei Autoinflammatory Disease (SPAID) 60,0 Spinal dysraphism 60,0 Spinocerebellar ataxia (SCA) 60,0 Spondylocostal dysostosis (Comma defect) 60,0 Spongy degeneration with cerebellar ataxia 60,0 Spongy degeneration with cerebellar ataxia 1 60,0 Startle disease 80,0 Subakute nekrotisierende Enzephalopathie(SNE) 60,0 Thrombopathia 60,0 Trapped neutrophil syndrome (TNS) 60,0 van den Ende-Gupta syndrome (VDEGS) 60,0 Vitamin D dependent rickets (VDR) 60,0 von-willebrand disease type I (vwd1) 60,0 von-willebrand disease type II (vwd 2) 60,0 von-willebrand disease type III (vwd3) 60,0 Warburg micro syndrome 1 (WARBM1) 60,0 X-chromosomal severe immuno defiziency 60,0 X-linked myopathy (XL-MTM) 60,0 Test per pelo 60,0 A-locus (alleles: Ay, Aw, at, a) 60,0 B-locus (brown, chocolate, liver(nose)) 60,0 Coat length I (long or short hair) 60,0 Curly (curled hair) 60,0 D-locus D1 (dilution) 60,0 E-locus (yellow, lemon, red, cream, apricot) 60,0 EM-locus (melanistic mask) 60,0 Furnishing (wire hair) 60,0 K-locus (only the allele KB) 60,0 M-locus (atypicl merle, merle, cryptic merle)** 60,0 S-locus (piebald, white spotting) 60,0