Optimal Selection
Optimal Selection
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Wisdom Panel
®
 3.0 Canine Genetic Test

PRICE: $99.99
Purchase for US Residents Only
Mars Veterinary, the makers of Optimal Selection™ have partnered with Genoscoper Laboratories® of Finland to provide breeders with the ability to test for both breed-specific diseases and genetic diversity. Maintaining and increasing genetic diversity, may reduce the occurrence of inherited diseases and other known issues that can result from inbreeding.

Testing for genetic diversity can help breeders decrease the incidence of producing affected puppies with recessively inherited diseases, by reducing the likelihood of mating two carriers of the same disease to produce afflicted offspring. Optimal Selection offers breeders the world's first dog matchmaking tool that helps estimate the genetic impact of the planned mating pair on the puppies.

In order to maintain comprehensive breed health, along with the use of Optimal Selection, it is important to consider:
  1. Other health information from phenotypic tests, such as hip and eye examinations.
  2. Physical and behavioral characteristics of the breeding dogs.
  3. Results of any other applicable tests or competitive titles in the breed.
  4. Any additional recommendations for potential breeding dogs that may be outlined by the breed club.
 
To view a sample Optimal Selection™ report click here. This report is for a sample dog named "Optimus Canine". When you get to the page, do not click on any of the left-hand navigation. That will take you off the sample and you will not be able to get back in without revisiting this page and link. Feel free to share this link with other breeders you think may find this helpful.
 
1
OPEN SWAB SLEEVE – Peel back the edges of the swab sleeve about 1 inch (not all the way) and remove swab by holding its handle. Do not touch the bristles. Save the sleeve to place the swabs in for mailing.
2
COLLECT CHEEK CELLS – Firmly roll the swab’s bristles between the inner surface of the cheek and gums for about 15 seconds for each swab. NOTE: DO NOT let your dog eat anything or share a water dish with other dogs for about an hour before you do the test.
3
AIR DRY SWABS – Insert swab handle in the hole of the carton insert and allow swabs to dry for about five minutes. Repeat steps 1-3 for the second swab.
4
ACTIVATE YOUR KIT – Visit www.os.genoscoper.com/start and fill out all the information, check it for accuracy and submit. You will receive an Activation Code Number that you need to write on the back of your Sample ID Sticker.
5
REINSERT DRY SWABS – Reinsert both dry swabs into the protective sleeve they came in. DO NOT reseal as this can cause bacterial growth.
6
SEAL THE CARTON – Place the sleeve with the swabs back into the carton it came in and seal.
7
MAIL TEST TO LAB – Pre-paid shipping label has already been placed on the carton.  Simply seal and place with the outgoing mail. IN APPROXIMATELY 3-4 WEEKS FROM THE TIME THE SAMPLE REACHES THE LAB YOU WILL BE EMAILED A LINK TO VIEW YOUR REPORT.
Screen your dog for genetic mutations that can predict specific health conditions.  Optimal Selection™ currently tests for over 125 different mutations in each dog.  Note that not all genetic mutations have been associated with a clinical disorder in every breed, thus those tested mutations that are most likely to impact your breed are specifically highlighted in your dog’s results.  Following is a list of the breeds and the genetic mutations that are most relevant to the breed.  Unless otherwise noted the Multidrug Resistance 1 (MDR1) and Degenerative Myelopathy (DM) mutations are highlighted for every breed. This list is always being updated as new mutations are added to the panel and more disease validation information becomes available.
 
 

Affenpinscher

Afghan Hound

Airedale Terrier

Factor VII Deficiency

Factor IX Deficiency or Haemophilia B; Mutation Originally Found in Airedale Terrier

Akita

Akita Inu

Alaskan Husky

Alaskan Husky Encephalopathy (AHE)

Alaskan Klee Kai

Factor VII Deficiency

Alaskan Malamute

Polyneuropathy; Mutation Originally Found in Alaskan Malamute

Cone Degeneration (CD) or Achromatopsia

Alaskan Noble Companion Dog

Alentejo Mastiff

Alpine Dachsbracke

American Bulldog

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Neuronal Ceroid Lipofuscinosis 10 (NCL10)

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

American English Coonhound

American Eskimo Dog

American Foxhound

American Hairless Terrier

Primary Lens Luxation (PLL)

American Staffordshire Terrier

Cone-Rod Dystrophy 1 (crd1); Mutation Originally Found in American Staffordshire Terrier

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

American Water Spaniel

Anatolian Shepherd Dog

Anglo-Francais de Petite Venerie

Anglo-Russian Hound

Appenzell Cattle Dog

Ariegeois

Atlas Shepherd Dog

Australian Cattle Dog

Primary Lens Luxation (PLL)

Myotonia; Mutation Originally Found in Australian Cattle Dog

 Neuronal Ceroid Lipofuscinosis 8 (NCL8); rare variant

Australian Kelpie

Australian Shepherd

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related breeds Mutation

Cone Degeneration (CD) or Achromatopsia

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Neuronal Ceroid Lipofuscinosis 8 (NCL8); rare variant

Australian Silky Terrier

Australian Stumpy Tail Cattle Dog

Australian Terrier

Austrian Black And Tan Hound

Austrian Pinscher

Azawakh

Barbet

Basenji

Progressive Retinal Atrophy -Adult onset; Mutation Originally Found in Basenji

Pyruvate Kinase Deficiency of Erythrocyte; Mutation Originally Found in Basenji

Basset Artesien Normand

Basset Bleu de Gascogne

Basset Fauve de Bretagne

Basset Hound

 X-linked Severe Combined Immuno deficiency (XSCID); Mutation Originally Found in Basset Hound

Bavarian Mountain Scenthound

Beagle

Osteogenesis imperfecta; Mutation Originally Found in Beagle

Factor VII Deficiency

Primary Open Angle Glaucoma; Mutation Originally Found in Beagle

Hypocatalasia or Acatalasemia

Musladin-Lueke syndrome (MLS)

Cerebellar Abiotrophy or neonatal Cerebellar Cortical Degeneration (NCCD)

Pyruvate Kinase Deficiency of Erythrocyte; Mutation Originally Found in Beagle

Imerslund-Grv§sbeck Syndrome (IGS) or Intestinal Cobalamin Malabsorbtion; Mutation Originally Found in Beagle

Bearded Collie

Beauceron

Bedlington Terrier

Belgian Groenendael

Belgian Laekenois

Belgian Malinois

Belgian Mastiff

Belgian Shepherd Dog

Belgian Tervueren

Bergamasco

Bernese Hound

Bernese Mountain Dog

Bichon Frise

Biewer Terrier

Black and Tan Coonhound

Black Russian Terrier

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Bloodhound

Blue Picardy Spaniel

Blue Tick Coonhound

Boerboel

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Bohemian Shepherd

Bolognese

Bolonka

Border Collie

Trapped Neutrophil Syndrome (TNS)

Imerslund-Grv§sbeck Syndrome (IGS) or Intestinal Cobalamin Malabsorbtion; Mutation Originally Found in Border Collie

Border Terrier

Borzoi

Bosnian Coarsehaired Hound

Boston Terrier

Bouvier des Ardennes

Bouvier des Flandres

Exercise-Induced Collapse (EIC)

Boxer

Factor VIII Deficiency or Haemophilia A; Mutation Originally Found in Boxer

Boykin Spaniel

Exercise-Induced Collapse (EIC)

Bracco Italiano

Braque d'Auvergne

Braque de l'Ariege

Braque du Bourbonnais

Braque Francais, type Gascogne

Braque Francais, type Pyrenees

Braque Saint-Germain

Briard

Briquet Griffon Vendeen

Brittany

Complement 3 (C3) Deficiency

Broholmer

Bull Terrier

Polycystic Kidney Disease (PKD)

Bulldog

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Bullmastiff

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Burgos Pointing Dog

Buryat-Mongol Dog

Cairn Terrier

GloboidCell Leukodystrophy (GLD) or Krabbe's Disease; Terrier Mutation

Congenital Macrothrombocytopenia; Disease-linked SNP Originally Found in Norfolk and Cairn Terrier

Craniomandibular Osteopathy (CMO)

Canaan Dog

Canadian Eskimo Dog

Cane Corso

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Cao de Castro Laboreiro

Cao Fila de Sao Miguel

Cardigan Welsh Corgi

X-linked Severe Combined Immuno deficiency (XSCID); Mutation Originally Found in Cardigan Welsh Corgi

Rod-Cone Dysplasia 3 (rcd3)

Catahoula Leopard Dog

Catalan Sheepdog

Caucasian Shepherd Dog

Cavalier King Charles Spaniel

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID)

Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD)

Episodic Falling (EF)

Central Asian Ovcharka

Ceskoslovensky Vlcak

Cesky Fousek

Cesky Terrier

Chesapeake Bay Retriever

Exercise-Induced Collapse (EIC)

Chien d'Artois

Chihuahua

Chinese Crested Dog

Primary Lens Luxation (PLL)

Chinese Shar Pei

Chinook

Chow Chow

Elliptocytosis

Ciobanesc Romanesc de Bucovina

Cirneco Dell'Etna

Clumber Spaniel

Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency

Exercise-Induced Collapse (EIC)

Cocker Spaniel

Glycogen Storage Disease VII or Hereditary Phosphofructokinase (PFK) Deficiency

Exercise-Induced Collapse (EIC)

Collie

Canine Cyclic Neutropenia; Cyclic Hematopoiesis; Gray Collie Syndrome (CN)

Coton de Tulear

Primary hyperoxaluria (PH); Mutation Originally Found in Coton de Tulear

Bandera's Neonatal Ataxia (BNAt)

Canine Multifocal Retinopathy 2 (CMR2); Mutation Originally Found in Coton de Tulear

Croatian Sheepdog

Curly Coated Retriever

Exercise-Induced Collapse (EIC)

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Glycogen Storage Disease type III a (GSD IIIa)

Dachshund -Miniature Longhaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Osteogenesis imperfecta (OI) or Brittle Bone Disease; Mutation Originally Found in Dachshund

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dachshund -Miniature Shorthaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Osteogenesis imperfecta (OI) or Brittle Bone Disease; Mutation Originally Found in Dachshund

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dachshund -Miniature Wirehaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy; Standard Wirehaired Dachshund (crd SWD)

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Osteogenesis imperfecta (OI) or Brittle Bone Disease; Mutation Originally Found in Dachshund

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dachshund - Standard Longhaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Osteogenesis imperfecta (OI) or Brittle Bone Disease; Mutation Originally Found in Dachshund

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dachshund - Standard Shorthaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dachshund - Standard Wirehaired

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in Dachshund

Cone-Rod Dystrophy; Standard Wirehaired Dachshund (crd SWD)

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Osteogenesis imperfecta (OI) or Brittle Bone Disease; Mutation Originally Found in Dachshund

Neuronal Ceroid Lipofuscinosis 1 (NCL1)

Dalmatian

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Dandie Dinmont Terrier

Danish-Swedish Farmdog

Primary Lens Luxation (PLL)

Deerhound

Factor VII Deficiency

Dobermann

Narcolepsy; Mutation Originally Found in Doberman Pinscher

Dilated Cardiomyopathy; Mutation Originally Found in Doberman Pinscher (USA)

Dogo Argentino

Dogo Canario

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Dogue de Bordeaux

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Drever

Dunker Hound

Dutch Shepherd Dog

East-European Shepherd

East-Siberian Laika

English Cocker Spaniel

Glycogen Storage Disease VII or Hereditary Phosphofructokinase (PFK) Deficiency

Autosomal Recessive Hereditary Nephropathy (ARHN); Mutation Originally Found in  English Cocker Spaniel

English Foxhound

English Pointer

English Setter

Neuronal Ceroid Lipofuscinosis 8 (NCL8)

English Springer Spaniel

Glycogen Storage Disease VII or Hereditary Phosphofructokinase (PFK) Deficiency

Autosomal Recessive Hereditary Nephropathy (ARHN); Mutation Originally Found in English Springer Spaniel

Shaking Puppy (X-linked Generalized Tremor); Mutation Originally Found in English Springer Spaniel

Cone-Rod Dystrophy (cord1-PRA /Crd4)

English Toy Terrier

Entlebucher Mountain Dog

Estonian Hound

Estrela Mountain Dog

Eurasier

Field Spaniel

Fila Brasileiro

Finnish Hound

Factor VII Deficiency

Finnish Lapphund

Glycogen Storage Disease Type II (GSD II) or Pompe's Disease

Finnish Spitz

Flat Coated Retriever

Fox Terrier - Smooth

Spinocerebellar Ataxia with Myokymia and/or seizures

Fox Terrier - Wire

Primary Lens Luxation (PLL)

Francais Blanc et Noir

Francais Blanc et Orange

Francais Tricolore

French Bulldog

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

French Spaniel

Frisian Water Dog

Severe Combined Immunodeficiency (SCID); Mutation Originally Found in Frisian Water Dog

German Hound

German Hunting Terrier

Primary Lens Luxation (PLL)

German Longhaired Pointer

German Pinscher

German Rough-haired Pointer

German Shepherd Dog

Factor VIII Deficiency or Haemophilia A; Mutation Originally Found in German Shepherd Dog

Factor VIII Deficiency or Haemophilia A; P.Cys548Tyr Mutation Originally Found in German Shepherd

Mucopolysaccharidosis Type VII (MPS VII); Mutation Originally Found in German Shepherd

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND)

Anhidrotic Ectodermal Dysplasia or X-linked Ectodermal Dysplasia (XHED)

German Shorthaired Pointer

Cone Degeneration (CD) or Achromatopsia; Mutation Originally Found in  German Shorthaired Pointer

von Willebrand's Disease (vWD) Type II

German Spaniel

German Spitz

German Wirehaired Pointer

von Willebrand's Disease (vWD) Type II

Exercise-Induced Collapse (EIC)

Giant Schnauzer

Factor VII Deficiency

Fetal-onset NeuroaxonalDystrophy (FNAD)

Hyperuricosuria And Hyperuricemia (HUU) or Urolithiasis

Golden Retriever

Golden Retriever Ichthyosis

Epidermolysis bullosa; Dystrophic

Muscular Dystrophy; Duchenne type or Golden Retriever Muscular Dystrophy (GRMD)

Golden Retriever Progressive Retinal Atrophy 1 (GR_PRA 1)

Golden Retriever Progressive Retinal Atrophy 2 (GR_PRA 2)

Gordon Setter

Cerebellar Ataxia; Mutation Originally Found in Old English Sheepdog and Gordon Setter

Gotland Hound

Grand Anglo-Francais

Grand Basset Griffon Vendeen

Grand Bleu de Gascogne

Grand Gascon Saintongeois

Grand Griffon Vendeen

Great Dane

Centronuclear Myopathy (CNM); Mutation Originally Found in Great Dane

Greater Swiss Mountain Dog

Bleeding Disorder Due to P2RY12 Defect

Greenland Dog

Greyhound

Polyneuropathy; Mutation Originally Found in Greyhound

Griffon Belge

Griffon Bleu de Gascogne

Griffon Bruxellois

Griffon Fauve de Bretagne

Griffon Nivernais

Halden Hound

Hälleforshund

Hamilton Hound

Hanoverian Scenthound

Harrier

Havanese

Hellenic Hound

Hokkaido

Hollandse Smoushond

Hovawart

Hungarian Greyhound

Hygen Hound

Ibizan Hound

Icelandic Sheepdog

Irish Glen of Imaal Terrier

Irish Red And White Setter

Irish Red Setter

Globoid Cell Leukodystrophy (GLD) or Krabbe's Disease; Mutation Originally Found in Irish Setter

Irish Soft Coated Wheaten Terrier

Irish Terrier

Hereditary Footpad Hyperkeratosis (HFH)

Irish Water Spaniel

Irish Wolfhound

Hyperekplexia or Startle Disease

Istrian Shorthaired Scent Hound

Istrian Wired-haired Scent Hound

Italian Greyhound

Amelogenesis Imperfecta (AI)

Italian Rough-haired Hound

Italian Shorthaired Hound

Jack Russell Terrier

Primary Lens Luxation (PLL)

Autosomal Recessive Severe Combined Immunodeficiency (ARSCID)

Spinocerebellar Ataxia with Myokymia and/or seizures

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Lamellar Ichthyosis (LI)

Spinocerebellar Ataxia (SCA); Mutation Originally Found in Parson Russell Terrier

Japanese Chin

GM2 Gangliosidosis; Mutation Originally Found in Japanese Chin

Japanese Spitz

Japanese Terrier

Jura Hound

Kai

Karelian Bear Dog

Chondrodysplasia; Mutation Originally Found in Norwegian Elkhound And Karelian Bear Dog

Karst Shepherd Dog

Keeshond

Kerry Blue Terrier

King Charles Spaniel or English Toy Spaniel

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis (CKCSID)

Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD)

Episodic Falling (EF)

Kishu

Komondor

Kooikerhondje

Koolie

Kopo

Korea Jindo Dog

Kromfohrländer

Hereditary Footpad Hyperkeratosis (HFH)

Kuvasz

Labrador Retriever

Exercise-Induced Collapse (EIC)

Hereditary Nasal Parakeratosis (HNPK)

Skeletal Dysplasia 2 (SD2)

Centronuclear Myopathy (CNM); Mutation Originally Found in Labrador Retriever

Myotubular Myopathy 1 or X-linked Myotubular Myopathy

Hyperuricosuria And Hyperuricemia (HUU) or Urolithiasis

Golden Retriever Progressive Retinal Atrophy 2 (GR_PRA 2)

Elliptocytosis

Pyruvate Kinase Deficiency of Erythrocyte; Mutation Originally Found in Labrador Retriever

Lagotto Romagnolo

Benign Familial Juvenile Epilepsy or Remitting Focal Epilepsy

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Lagotto Storage Disease

Lakeland Terrier

Lancashire Heeler

Primary Lens Luxation (PLL)

Landseer

Cystinuria; Mutation Originally Found in Newfoundland Dog

Lapponian Herder

Canine Multifocal Retinopathy 3 (CMR3); Mutation Originally Found in Lapponian Herder

Glycogen Storage Disease Type II (GSD II) or Pompe's Disease

Large Münsterländer

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Leonberger

Lhasa Apso

Factor IX Deficiency or Haemophilia B; Mutation Originally Found in Lhasa Apso

Longhaired Whippet

Löwchen

Lucerne Hound

Majorca Mastiff

Majorca Shepherd Dog

Maltese

Glycogen Storage Disease; Type Ia (GSD Ia)

Manchester Terrier

Manchester Terrier - Toy

Maremma and Abruzzes Sheepdog

Mastiff

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Mi-ki

Miniature Bull Terrier

Polycystic Kidney Disease (PKD)

Primary Lens Luxation (PLL)

Miniature Pinscher

Miniature Schnauzer

Factor VII Deficiency

Myotonia; Mutation Originally Found in Miniature Schnauzer

Persistant Müllerian Duct Syndrome (PMDS) Mutation Originally Found in Miniature Schnauzer

Montenegrin Mountain Hound

Moscow Watchdog

Mudi

Neapolitan Mastiff

New Zealand Huntaway

Mucopolysaccharidosis Type IIIA (MPS IIIA); Mutation Originally Found in New Zealand Huntaway

Newfoundland

Cystinuria; Mutation Originally Found in Newfoundland Dog

Norfolk Terrier

Epidermolytic Hyperkeratosis or Ichthyosis in Norfolk Terrier

Congenital Macrothrombocytopenia; Disease-linked SNP Originally Found in Norfolk And Cairn Terrier

Norrbottenspitz

Norwegian Buhund

Norwegian Elkhound

von Willebrand's Disease (vWD) Type II

Chondrodysplasia; Mutation Originally Found in Norwegian Elkhound And Karelian Bear Dog

Early Retinal Degeneration; Mutation Originally Found in Norwegian Elkhound

Glaucoma; Mutation Originally Found in Norwegian Elkhound

Norwegian Lundehund

Norwich Terrier

Epidermolytic Hyperkeratosis or Ichthyosis in Norfolk Terrier

Primary Lens Luxation (PLL)

Nova Scotia Duck Tolling Retriever

Old Danish Pointing Dog

Congenital Myasthenic Syndrome (CMS)

Old English Sheepdog

Exercise-Induced Collapse (EIC)

Primary Ciliary Dyskinesia (PCD)

Cerebellar Ataxia; Mutation Originally Found in Old English Sheepdog and Gordon Setter

Otterhound

Papillon

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Progressive Retinal Atrophy (PAP1_PRA); Mutation Originally Found in Papillon and Phalene

Parson Russell Terrier

Primary Lens Luxation (PLL)

Autosomal Recessive Severe Combined Immunodeficiency (ARSCID)

Spinocerebellar Ataxia with Myokymia and/or seizures

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Spinocerebellar Ataxia (SCA); Mutation Originally Found in Parson Russell Terrier

Partridge Dog

Patterdale Terrier

Primary Lens Luxation (PLL)

Pekingese

Pembroke Welsh Corgi

Exercise-Induced Collapse (EIC)

Rod-Cone Dysplasia 3 (rcd3)

Peruvian Hairless Dog - Large

Peruvian Hairless Dog -Medium sized

Peruvian Hairless Dog -Miniature

Petit Basset Griffon Vendeen

Petit Bleu de Gascogne

Petit Brabancon

Petit Gascon Saintongeois

Phalene

Cone-Rod Dystrophy (cord1-PRA /Crd4)

Progressive Retinal Atrophy (PAP1_PRA); Mutation Originally Found in Papillon and Phalene

Pharaoh Hound

Picardy Sheepdog

Picardy Spaniel

Plott

Podenco Canario

Poitevin

Polish Greyhound

Polish Hound

Polish Hunting Dog

Polish Lowland Sheepdog

Pomeranian

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Hereditary Vitamin D-Resistant Rickets (HVDRR)

Poodle - Miniature

Osteochondrodysplasia; Mutation Originally Found in Miniature Poodle

Poodle - Standard

Osteochondrodysplasia; Mutation Originally Found in Miniature Poodle

Neonatal Encephalopathy with Seizures (NEWS)

Poodle - Toy

Osteochondrodysplasia; Mutation Originally Found in Miniature Poodle

GM2 Gangliosidosis; Mutation Originally Found in Toy Poodle

Porcelaine

Portuguese Podengo

Portuguese Pointing Dog

Portuguese Sheepdog

Portuguese Water Dog

Posavski Gonic

Pražký Krysarík

Pudelpointer

Pug

May-Hegglin Anomaly (MHA)

Pyruvate Kinase Deficiency of Erythrocyte; Mutation Originally Found in Pug

Puli

Pumi

Primary Lens Luxation (PLL)

Pyrenean Mastiff

Pyrenean Mountain Dog or Great Pyrenees

Canine Multifocal Retinopathy 1 (CMR1); Mastiff-related Breeds Mutation

Glanzmann Thrombasthenia (GT) Type I; Mutation Originally Found in Pyrenean Mountain Dog

Pyrenean Sheepdog

Rat Terrier

Congenital Hypothyroidism; Mutation Originally Found in Toy Fox and Rat Terrier

Primary Lens Luxation (PLL)

Ratonero Bodeguero Andaluz

Redbone Coonhound

Rhodesian Ridgeback

Romanian Carpathian Shepherd Dog

Romanian Mioritic Shepherd Dog

Rottweiler

Russian Hound

Russian Toy Dog

Russian-European Laika

Saarloos Wolfdog

Saint Bernard

Saluki

Samoyed

X-linked Hereditary Nephropathy (XLHN)

Sarplaninac

Schapendoes

Schiller Hound

Schipperke

Schwyz Hound

Scottish Terrier

Craniomandibular Osteopathy (CMO)

Sealyham Terrier

Primary Lens Luxation (PLL)

Serbian Hound

Serbian Tricolour Hound

Shetland Sheepdog

Shiba

Shih Tzu

Prekallikrein Deficiency

Shikoku

Siberian Husky

Silken Windhound

Skye Terrier

Sloughi

Rod-Cone Dysplasia 1a (rcd1a); Mutation Originally Found in Sloughi

Slovakian Chuvach

Slovakian Hound

Slovakian Wirehaired Pointing Dog

Smaland Hound

Small Bernese Hound

Small Jura Hound

Small Lucerne Hound

Small Münsterländer

Small Schwyz Hound

South Russian Ovcharka

Spaniel de Pont-Audemer

Spanish Greyhound

Spanish Hound

Spanish Mastiff

Spanish Water Dog

Spinone Italiano

Stabyhoun

Staffordshire Bull Terrier

L-2-Hydroxyglutaric Aciduria (L2HGA); Mutation 1 Originally Found in Staffordshire Bull Terrier

L-2-Hydroxyglutaric Aciduria (L2HGA); Mutation 2 Originally Found in Staffordshire Bull Terrier

Standard Schnauzer

Steirische Rauhhaarbracke

Sussex Spaniel

Pyruvate Dehydrogenase Phosphatase 1 (PDP1) Deficiency

Swedish Elkhound

Swedish Lapphund

Glycogen Storage Disease Type II (GSD II) or Pompe's Disease

Swedish Vallhund

Swedish White Elkhound

Swiss Hound

Taigan

Taiwan Dog

Tamaskan Dog

Tatra Shepherd Dog

Tenterfield Terrier

Spinocerebellar Ataxia with Myokymia and/or seizures

Terrier Brazileiro

Mucopolysaccharidosis Type VII (MPS VII); Mutation Originally Found in Brazilian Terrier

Thai Bangkaew Dog

Thai Ridgeback

Tibetan Mastiff

Tibetan Spaniel

Progressive Retinal Atrophy (PRA) type III; Mutation Originally Found in Tibetan Spaniel and Tibetan Terrier

Tibetan Terrier

Primary Lens Luxation (PLL)

Adult-Onset Neuronal Ceroid Lipofuscinosis (Adult-onset NCL) Mutation Originally Found in Tibetan terrier

Progressive Retinal Atrophy (PRA) type III; Mutation Originally Found in Tibetan Spaniel and Tibetan Terrier

Tiroler Bracke

Tornjak

Tosa

Toy Fox Terrier

Congenital Hypothyroidism; Mutation Originally Found in Toy Fox And Rat Terrier

Primary Lens Luxation (PLL)

Spinocerebellar Ataxia with Myokymia and/or seizures

Treeing Walker Coonhound

Uruguayan Cimarron

Vizsla

Vizsla - Wirehaired

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Volpino Italiano

Primary Lens Luxation (PLL)

Weimaraner

Hypomyelination and Tremor; Mutation Originally Found in Weimaraner

Hyperuricosuria and Hyperuricemia (HUU) or Urolithiasis

Welsh Springer Spaniel

Factor VII Deficiency

Welsh Terrier

Primary Lens Luxation (PLL)

West Highland White Terrier

Globoid Cell Leukodystrophy (GLD) or Krabbe's Disease; Terrier Mutation

Pyruvate Kinase Deficiency of Erythrocyte; Mutation Originally Found in West Highland White Terrier

Craniomandibular Osteopathy (CMO)

Westphalian Dachsbracke

West-Siberian Laika

Whippet

Muscular Hypertrophy (double Musculing)

Glycogen Storage Disease VII or Hereditary Phosphofructokinase (PFK) Deficiency

White Swiss Shepherd Dog

Wirehaired Pointing Griffon Korthals

Xoloitzcuintle

Yakutian Laika

Yorkshire Terrier

Primary Lens Luxation (PLL)

 

 
 

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