L Locus (Long Hair/Fluffy), Lh1 (Common Variant Found in Many Breeds), L locus, long hair trait, longhaired trait, short hair trait, shorthaired trait

Collie Cyclic Neutropenia (CN)

Cyclic Hematopoiesis, Gray Collie Syndrome, CH

Congenital Myasthenic Syndrome, Labrador Type (CMS-LAB)

CMS-LAB

April 11, 2023

Copper Toxicosis Labrador Retriever ATP7A (CT-LAB-A)

Copper Hepatoxicosis, Copper Storage Disease, Copper Storage Disease Modifier, Copper Storage Hepatitis, Copper-associated Hepatopathy, Hepatic Copper Toxicosis, Menkes Gene Disease Modifier, Wilson Disease

April 6, 2023

Copper Toxicosis Labrador Retriever ATP7B (CT-LAB-B)

Curl-Locus (CURL)

Cu Locus, Curly Hair, Curly Coat Trait, Straight Coat Trait, Wavy Coat Trait

D-Locus (D-LOCUS)

Dilution, Dilute Coat, Coat Color Dilution

Deafness with Vestibular Dysfunction 1 (DINGS1)

Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Congenital Hearing and Vestibular Disorder, DINGS, DVD

Deafness with Vestibular Dysfunction 2 (DINGS2)

Deafness and Vestibular Dysfunction (Doberman Pinscher Type), Congenital Hearing and Vestibular Disorder, DINGS, DVD

Degenerative Myelopathy (DM)

Canine Degenerative Myelopathy, SOD1A

Dilated Cardiomyopathy 1 (DCM1)

Dilated Cardiomyopathy, DCM

Dilated Cardiomyopathy 2 (DCM2)

Dilated Cardiomyopathy, DCM

Dominant PRA (PRA-D)

Progressive Retinal Atrophy (Bullmastiff/Mastiff Type)

Dry Eye Curly Coat Syndrome (CKCSID)

Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis

E-Locus (E-LOCUS)

E/e Locus, Extension Locus, Red Coat Color, Yellow Coat Color, Apricot/Cream/Red/Yellow

Early Onset Progressive Retinal Atrophy (EO-PRA)

Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type)

Episodic Falling (EF)

Episodic Falling Syndrome, Collapsing Cavaliers Syndrome, Exercise-induced paroxysmal hypertonicity, Falling Cavaliers Syndrome, Sudden Collapse Syndrome, EFS

Exercise Induced Collapse (EIC)

Exercise-Induced Collapse

Furnishings-Improper Coat Locus (FURN-IC-LOCUS)

Furnishings, Improper Coat, Wh Locus, Wire Hair Trait, Wirehaired Trait

Golden Retriever Progressive Retinal Atrophy 2 (GR-PRA2)

Progressive Retinal Atrophy, Golden Retriever 2, GR2-PRA

Hereditary Cataracts (HC)

Early onset cataracts, Juvenile cataracts, HC, HSF4, JC

Hereditary Nasal Parakeratosis (HNPK)

Hereditary Nasal Parakeratosis (Labrador Retriever Type)

Hyperuricosuria (HU)

Urolithiasis, HUU

Ichthyosis-A (ICT-A)

Ichthyosis (Golden Retriever Type 1)

Imerslund-Gräsbeck Syndrome, Beagle Type (IGS-BEA)

Cobalamin Deficiency, Cubilin Deficiency, Imerslund-Grasbeck Syndrome, Vitamin B12 Deficiency, I-GS

Imerslund-Gräsbeck syndrome, Border Collie Type (IGS-BORD)

Cobalamin Deficiency, Cubilin Deficiency, Imerslund-Grasbeck Syndrome, Vitamin B12 Deficiency, I-GS

Irish Setter PRA Type 1 (PRA-RCD1)

Progressive Retinal Atrophy (Irish Setter Type), Rod-Cone Dysplasia 1, PRA-rcd1

K-KB-Locus (K-KB-LOCUS)

K Locus (Dominant Black), Agouti Expression Locus, Dominant Black Coat Color, K Locus, KB Locus, ky Locu

Labrador Centronuclear Myopathy (CNM)

Hereditary Myopathy of the Labrador Retriever, Type II Muscle Fiber Deficiency

Laryngeal Paralysis (LP)

Laryngeal Paralysis (Bull Terrier Type)

Lethal Acrodermatitis (LAD)

Lethal Acrodermatitis MKLN1 (Bull Terrier Type), Genodermatosis

Merle-Locus (MERLE)

M Locus (Merle), Merle Coat Color

Microphthalmia (MAC)

Canine Congenital Eye Disease, Multiple Ocular Defects with Microphthalmia, MAC

Multidrug Sensitivity (MDR1)

Multidrug Resistance 1, Ivermectin Sensitivity, MDR1 gene defect

Neonatal Encephalopathy (NE)

Neonatal Encephalopathy with Seizures, NEWS, Neonatal Encephalopathy (Poodle Type)

Neuraxonal Dystrophy Papillon Type (NAD-PAP)

Neuronal Dystrophy, NAD

Neuroaxonal Dystrophy Spanish Water Dog (NAD-SWD)

Neuronal Dystrophy, NAD

Newfoundland Cystinuria (CYS)

Type IA Cystinuria, Cystinuria (Newfoundland Type)

Osteochondrodysplasia (OCD)

Skeletal dwarfism

Osteogenesis Imperfecta Dachshund (OI-DACH)

Brittle Bone Disease, OI

April 19, 2023

Papillon PRA Type 1 (PAP-PRA1)

Progressive Retinal Atrophy PRA1 (Papillon Type), Progressive Retinal Atrophy 1, PRA, PRA1

April 6, 2023

Persistent Mullerian Duct Syndrome (PMDS)

PMDS

Phosphofructokinase Deficiency (PFK)

Glycogen Storage Disease VII, PFK Deficiency, Glycogen Storage Disease VII, Glycogenosis Type VII, GSD VII, PFKM, Tarui-Layzer Syndrome

PRA-CORD1-CRD4 (PRA-CORD1-CRD4)

Progressive Retinal Atrophy, Cone-Rod Dystrophy 4, Progressive Retinal Atrophy-cord1, Progressive Retinal Atrophy-crd4, Progressive retinal atrophy-crd4/cord1, PRA-cord1, PRA-crd4, PRA-crd4/cord1