CAIRN TERRIER DNA test Results sent direct to KC Owner submission to KC Not recorded by the Kennel Club AB required AB rec'd Patent Genindexe

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1 CAIRN TERRIER Globoid Cell Leukodystrophy (GCL) Pyruvate Kinase Deficiency Craniomandibular Osteopathy (CMO) Gallbladder Mucocele Formation PennGen Canine Mask test CANAAN DOG Degenerative Myelopathy (DM) CAVALIER KING CHARLES SPANIEL Curly Coat / Dry Eye AHT

2 (CC/DE) YES Episodic Falling (EF) AHT YES Muscular Dystrophy (MD) Thrombocytopaenia Degenerative Myelopathy (DM) Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, (CKCSID) Phosphofructokinase deficiency (PFK) CHIHUAHUA (LONG & SMOOTH COAT) Thrombocytopaenia Progressive Retinal Atophy crd4 Progressive Retinal Atrophy prcd Lipofuscinosis, (NCL7)

3 Spirocerebllar Ataxia (SCA) Coat length (Long hair gene) Curly hair Genetic Technologies (Animal Network) CHINESE CRESTED * Progressive Retinal Atrophy, * Genetic Technologies (Animal Network)* YES YES prcd (prcd-pra) * * * van Haeringen * Primary Lens Luxation AHT Genetic Technologies (Animal Network) (PLL) YES Degenerative Myelopathy (DM) Lipofuscinosis, (NCL7) von Willebrand's disease (vwd) Type 2 Canine Multiple System Degeneration (CMSD) Coat length / texture AHT

4 Coat colour gene variations CHOW CHOW Degenerative Myelopathy (DM) Elliptocytosis Coat length / texture COLLIE (ROUGH) * Collie Eye Anomaly/ * Genetic Technologies (Animal Network)* YES YES Choroidal Hypoplasia * (CEA/CH)* * * AHT Genetic Technologies (Animal Network) Multi Drug Resistance YES (MDR1) Lipofuscinosis (NCL) Progressive Retinal Atrophy,

5 rcd2 (PRA-rcd2) Degenerative Myelopathy (DM) von Willebrands disease II Dermatomyositis (DMS) Hyperuricursuria (HUU) Canine Cyclic Neutropenia (CNN) Canine coat and nose colour Genetic Technologies (Animal Network) Vetgen COLLIE (SMOOTH) * Collie Eye Anomaly/ * Genetic Technologies (Animal Network)* YES YES Choroidal Hypoplasia * (CEA/CH)* * * Multi Drug Resistance AHT YES (MDR1) Lipofuscinosis (NCL) Progressive Retinal Atrophy, rcd2 (PRA-rcd2)

6 Degenerative Myelopathy (DM) Canine Cyclic Neutropenia (CNN) Dermatomyositis (DMS) von Willebrands disease II Genetic Technologies (Animal Network) Hyperuricursuria (HUU) Canine coat and nose colour COTON DE TULEAR Hyperuricosuria (HUU) Degenerative Myelopathy (DM) von Willebrand's disease (vwd) Type 1 von Willebrand's disease

7 (vwd) Type 3 Cerebellar Ataxia (CA) Bander's Neonatal Ataxia Canine Multifocal Retinopathy (CMR) Primary Hyperoxaluria (PH) Coat colour Animal DNA Dianostics DACHSHUND (LONG-HAIRED) Multi Drug Resistance (MDR1) Progressive Retinal Atrophy cord1 (PRA-cord1)

8 Mucopolysaccharidosis (MPS) IIIA Lipofuscinosis 1 Lipofuscinosis 2 Narcolepsy Pyruvate Kinase Deficiency (PKD) Osteogenesis Imperfecta Long Hair Gene (Hair length) PennGenn PennGenn Animal DNA Diagostics Animal DNA Diagostics

9 DACHSHUND (MINIATURE LONG-HAIRED) Progressive Retinal Atrophy AHT Genetic Technologies (Animal Network) cord1 (PRA-cord1) YES OFFA Mucopolysaccharidosis (MPS) IIIA PennGenn Multi Drug Resistance (MDR1) Narcolepsy Lipofuscinosis 1 Lipofuscinosis 2 Osteogenesis Imperfecta Long Hair Gene (Hair length)

10 Coat Length (Texture) Genetic Technologies (Animal Network) Animal DNA DIagostics DACHSHUND (MINIATURE SMOOTH-HAIRED) AHT Progressive Retinal Atrophy YES cord1 (PRA-cord1) Mucopolysaccharidosis PennGenn (MPS) IIIA Narcolepsy Multi Drug Resistance (MDR1) Pyruvate Kinase Deficiency (PKD) Osteogenesis Imperfecta PennGenn

11 Coat Length (Texture) Animal DNA DIagostics DACHSHUND (MINIATURE WIRE-HAIRED) Lafora's Disease Hospital for Sick Children YES AHT Genetic Technologies (Animal Network) Progressive Retinal Atrophy YES cord1 (PRA-cord1) Lipofuscinosis (NCL) Mucopolysaccharidosis (MPS) IIIA PennGenn Multi Drug Resistance (MDR1) Narcolepsy Osteogenesis Imperfecta

12 Progressive Retinal Atrophy CRD (NHPH4) Coat Length (Texture) AHT Animal DNA Diagostics Animal DNA Diagostics DACHSHUND (WIRE-HAIRED) Genoscoper Multi Drug Resistance (MDR1) Progressive Retinal Atrophy cord1 (PRA-cord1) Progressive Retinal Atrophy cord2 (PRA-cord2) Lipofuscinosis 1 Lipofuscinosis 2 Mucopolysaccharidosis (MPS) IIIA Narcolepsy

13 Osteogenesis Imperfecta Progressive Retinal Atrophy CRD (NHPH4) Factor VII Deficiency Long Hair gene (hair length) AHT DALMATIAN Hyperuricosuria (HUU)** AHT ** conditions apply ** please refer to the Health & Breeder Services Dept at the KC for more information Degenerative Myelopahy (DM) Acute Respiratory Distress Syndrome (ARDS)

14 Canine Coat & Nose colour Coat colour Coat length / texture DANDIE DINMONT TERRIER Canine Coat & Nose colour DEERHOUND von Willebrand's Disease (vwd) Type 1 Factor VII Deficiency Long Hair gene (hair length) AHT PennGenn

15 Coat colour DOBERMANN von Willebrand's disease Genetic Technologies (Animal Network) (vwd) Type 1 YES Dilated Cardiomyopathy (DCM) Narcolepsy Bobtail gene White Dobermann causing Oculocutaneous Albinism Genetic Technologies (Animal Network) Canine Coat & Nose colour Coat colour Animal DNA Dianostics

16 DOGUE DE BORDEAUX Canine Multifocal Retinopathy (CMR1) Digital Hyperkeratosis (DH) (Hereditary Footpad Hyperkeratosis/Corny feet) Focal Non-Epidermolytic Palmoplantar Keratoderma (FNEPPK) Coat colour

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