A

  • Adult-onset neuronal ceroid lipofuscinosis

    Amaurotic idiocy, Batten disease, NCL

  • Alaskan Husky encephalopathy

    Subacute necrotizing encephalomyelopathy, AHE

  • Alaskan Malamute polyneuropathy

    Hereditary polyneuropathy of Alaskan Malamutes, Inherited polyneuropathy, AMPN

  • Amelogenesis imperfecta

    Autosomal recessive amelogenesis imperfecta, Familial enamel hypoplasia, AI, ARAI

  • Anhidrotic ectodermal dysplasia

    Congenital hypotrichosis, Ectodermal dysplasia, X-linked ectodermal dysplasia, X-linked hypohidrotic ectodermal dysplasia, XHED, XLED

B

  • Benign familial juvenile epilepsy

    BFJE

C

  • Canine multiple system degeneration (Chinese Crested type)

    CMSD

  • Canine multiple system degeneration (Kerry Blue Terrier type)

    Progressive neuronal abiotrophy, CMSD, PNA

  • Cerebellar ataxia (Finnish Hound type)

    Progressive early onset ataxia

  • Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound type)

    Dwarfism

  • Coagulation factor VII deficiency

    Factor VII deficiency, Hypoproconvertinemia

  • Collie eye anomaly

    Choroidal hypoplasia, CEA, CH

  • Complement 3 deficiency

    C3 deficiency, Complement component 3 deficiency

  • Cone degeneration

    Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy, CD

  • Cone degeneration (German Shorthaired Pointer type)

    Achromatopsia, Day blindness, Hemeralopia, Rod monochromacy

  • Congenital hypothyroidism with goiter (Terrier type)

    CHG

  • Congenital myasthenic syndrome (Labrador Retriever type)

  • Congenital myasthenic syndrome (Old Danish Pointer type)

    CMS

  • Congenital stationary night blindness

    Hereditary retinal dystrophy, Leber congenital amaurosis, Retinal pigment epithelial dystrophy, CSNB, LCA

  • Cyclic neutropenia

    Cyclic hematopoiesis, Gray collie syndrome, CH, CN

  • Cystinuria (Australian Cattle Dog type)

    Autosomal dominant cystinuria, Type IIA cystinuria

  • Cystinuria (Miniature Pinscher type)

  • Cystinuria (Newfoundland type)

    Type IA cystinuria

D

  • Degenerative myelopathy

    Canine degenerative myelopathy, DM

  • Dilated cardiomyopathy

    DCM

  • Dry eye curly coat syndrome

    Congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, CKSID

  • Dystrophic epidermolysis bullosa

    Recessive dystrophic epidermolysis bullosa, DEB, EB, RDEB

E

  • Early retinal degeneration

    Progressive retinal atrophy-erd, Retinal photoreceptor dysplasia, ERD

  • Ectodermal dysplasia

  • Elliptocytosis

  • Epidermolytic hyperkeratosis

    Ichthyosis

  • Episodic falling syndrome

    Collapsing Cavaliers syndrome, Exercise-induced paroxysmal hypertonicity, Falling Cavaliers syndrome, Sudden collapse syndrome, EFS

  • Exercise-induced collapse

    EIC

F

  • Familial nephropathy (Cocker Spaniel type)

    Hereditary nephropathy, Nephropathy, FN, HN

  • Familial nephropathy (English Springer Spaniel type)

    Hereditary nephropathy, Nephropathy, FN, HN

  • Fanconi syndrome

    Fanconi's syndrome, Paradoxic glucosuria

G

  • Gallbladder mucoceles

    Hepatobiliary disease, Mucinous cholecystitis, Mucinous hyperplasia

  • Glanzmann's thrombasthenia (Great Pyrenees type)

    Thrombasthenia, Thrombasthenic thrombopathia, GT

  • Glanzmann's thrombasthenia (Otterhound type)

    Thrombasthenia, Thrombasthenic thrombopathia, GT

  • Globoid cell leukodystrophy (Irish Setter type)

    Galactocerebrosidase deficiency, Krabbe disease, GLD

  • Globoid cell leukodystrophy (Terrier type)

    Galactocerebrosidase deficiency, Krabbe disease, GLD

  • Glycogen storage disease Ia

    Von Gierke disease, GSD Ia, GSD1a

  • Glycogen storage disease IIIa

    GSD IIIa

  • Glycogen storage disease VII (Wachtelhund type)

    Phosphofructokinase deficiency, GSD VII, PFK deficiency

  • GM1 Gangliosidosis (Alaskan Husky type)

  • GM1 Gangliosidosis (Portuguese Water Dog type)

  • GM1 Gangliosidosis (Shiba Inu type)

  • GM2 Gangliosidosis (Japanese Chin type)

    Sandhoff disease, Tay-Sachs disease, Type 0 gangliosidosis

  • GM2 Gangliosidosis (Poodle type)

    Sandhoff disease, Type 0 gangliosidosis

  • Greyhound polyneuropathy

    Hereditary neuropathy

H

  • Hemophilia A (Boxer type)

  • Hemophilia A (German Shepherd Dog, type 1)

  • Hemophilia A (German Shepherd Dog, type 2)

    Factor VIII deficiency

  • Hemophilia B (Cairn Terrier type)

    Christmas disease, Factor IX deficiency

  • Hemophilia B (Lhasa Apso type)

    Christmas disease, Factor IX deficiency

  • Hemophilia B (Rhodesian Ridgeback type)

    Christmas disease, Factor IX deficiency

  • Hereditary cataracts

    Early onset cataracts, Juvenile cataracts, HC, JC

  • Hereditary cataracts (Australian Shepherd type)

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

  • Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type)

  • Hereditary nasal parakeratosis

    HNPK

  • Hereditary nephritis (Samoyed type)

    Alport syndrome, Samoyed hereditary glomerulopathy, X-linked nephritis, AS, HN, XLHN

  • Hyperuricosuria

    Urolithiasis, HUU

I

  • Ichthyosis (Golden Retriever type)

  • Inherited myopathy of Great Danes

    Central core myopathy, IMGD

  • Intestinal cobalamin malabsorption (Beagle type)

  • Intestinal cobalamin malabsorption (Border Collie type)

    Cobalamin deficiency, Cubilin deficiency, Imerslund-Grasbeck syndrome, I-GS

J

  • Juvenile Laryngeal Paralysis and Polyneuropathy

L

  • L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type)

    L-2-hydroxyglutaricacidemia, Organic aciduria, L-2-HGA

  • Late onset ataxia

    Spinocerebellar ataxia, LOA, SCA

  • Leukocyte adhesion deficiency, type I

    Canine Leukocyte Adhesion Deficiency, CLAD, LAD-I

  • Leukocyte adhesion deficiency, type III

    Canine leukocyte adhesion deficiency, Leukocyte/Platelet adhesion defect, CLAD, LAD-III

M

  • May-Hegglin anomaly

    MHA

  • Mucopolysaccharidosis I

    Alpha-L-iduronidase deficiency, Hurler syndrome, Scheie syndrome, MPS I

  • Mucopolysaccharidosis IIIA (Dachshund type)

    Sanfilippo syndrome type A, MPS IIIA

  • Mucopolysaccharidosis IIIA (New Zealand Huntaway type)

    Sanfilippo syndrome type A, MPS IIIA

  • Mucopolysaccharidosis VII (Shepherd type)

    Beta-glucuronidase deficiency, Sly Syndrome, MPS VII

  • Multidrug resistance 1

    Ivermectin sensitivity, MDR1 gene defect, Multidrug sensitivity, MDR1

  • Multifocal retinopathy 1

    Canine multifocal retinopathy 1, CMR1

  • Multifocal retinopathy 2

    Canine multifocal retinopathy 2, CMR2

  • Multifocal retinopathy 3

    Canine multifocal retinopathy 3, CMR3

  • Muscular Dystrophy (Golden Retriever Type)

    Duchenne-type muscular dystrophy, Dystrophin muscular dystrophy, DMD, GRMD

  • Musladin-Lueke syndrome

    Chinese Beagle Syndrome, MLS

  • Myostatin deficiency (Whippet and Longhaired Whippet type)

  • Myotonia congenita (Australian Cattle Dog type)

    Congenital myotonia, Inherited myotonia, Myotonia, Myotonia hereditaria

  • Myotonia congenita (Schnauzer type)

    Congenital myotonia, Inherited myotonia, Myotonia, Myotonia hereditaria

  • Myotubular myopathy 1

    X-linked myotubular myopathy, MTM1, XLMTM

N

  • Narcolepsy (Dachshund type)

  • Narcolepsy (Doberman Pinscher type)

  • Narcolepsy (Labrador Retriever type)

  • Neonatal cerebellar cortical degeneration

    Cerebellar abiotrophy, Cerebellar cortical degeneration, NCCD

  • Neonatal encephalopathy with seizures

    NEWS

  • Neuronal ceroid lipofuscinosis 1

    Amaurotic idiocy, Batten disease, NCL, NCL1

  • Neuronal ceroid lipofuscinosis 10

    Amaurotic idiocy, Batten disease, NCL, NCL10

  • Neuronal ceroid lipofuscinosis 2

    Amaurotic idiocy, Batten disease, NCL, NCL2

  • Neuronal ceroid lipofuscinosis 4A

    Amaurotic idiocy, Batten disease, cerebellar ataxia, NCL, NCL4A

  • Neuronal ceroid lipofuscinosis 5

    Amaurotic idiocy, Batten disease, NCL, NCL5

  • Neuronal ceroid lipofuscinosis 6

    Amaurotic idiocy, Batten disease, NCL, NCL6

  • Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type)

  • Neuronal ceroid lipofuscinosis 8 (Setter type)

    Amaurotic idiocy, Batten disease, NCL, NCL8

O

  • Osteochondrodysplasia

    Skeletal dwarfism, OCD

  • Osteogenesis imperfecta (Beagle type)

    Brittle bone disease, OI

  • Osteogenesis imperfecta (Dachshund type)

    Brittle bone disease, OI

  • Osteogenesis imperfecta (Golden Retriever type)

    Brittle bone disease, OI

P

  • P2RY12 receptor platelet disorder

    Platelet disorder of Greater Swiss Mountain Dog

  • Pembroke Welsh Corgi Duchenne muscular dystrophy

  • Persistent Müllerian duct syndrome

    PMDS

  • Polyneuropathy (Leonberger and Saint Bernard type)

  • Pompe disease

    Glycogen storage disease II, Pompe's disease, GSD II

  • Prekallikrein deficiency

    Fletcher factor deficiency, Fletcher trait

  • Primary ciliary dyskinesia

    Kartagner syndrome, PCD

  • Primary hyperoxaluria

    Oxalosis I, Primary hyperoxaluria I, PH1

  • Primary lens luxation

    Lens luxation, PLL

  • Primary open angle glaucoma

    POA glaucoma

  • Progressive retinal atrophy (Basenji type)

    Adult-onset progressive retinal atrophy, Basenji retinopathy

  • Progressive retinal atrophy (Bullmastiff/Mastiff type)

    PRA-D

  • Progressive retinal atrophy (Irish Setter type)

    Rod-cone dysplasia 1, PRA-rcd1

  • Progressive retinal atrophy (Sloughi type)

    Rod-cone dysplasia 1a, PRA-rcd1a

  • Progressive retinal atrophy, Cone-rod dystrophy 1

  • Progressive retinal atrophy, Cone-rod dystrophy 2

    PRA-crd2

  • Progressive retinal atrophy, Cone-rod dystrophy 3

    PRA-crd3

  • Progressive retinal atrophy, generalized

    gPRA

  • Progressive retinal atrophy, Golden Retriever 1

    GR-PRA1, GR1-PRA

  • Progressive retinal atrophy, Golden Retriever 2

    GR-PRA2, GR2-PRA

  • Progressive retinal atrophy, PRA1 (Papillon type)

    Progressive retinal atrophy 1, PRA, PRA1

  • Progressive retinal atrophy, Progressive rod-cone degeneration

    PRA-PRCD, PRCD

  • Progressive retinal atrophy, Rod-cone dysplasia 3

    Rod-cone dysplasia 3, PRA-rcd3

  • Pyruvate dehydrogenase deficiency

    Pyruvate dehydrogenase phosphatase 1 deficiency, Pyruvate dehydrogenase phosphatase deficiency, PDP1 deficiency

  • Pyruvate kinase deficiency (Basenji type)

    Pyruvate kinase deficiency of erythrocytes, PK deficiency

  • Pyruvate kinase deficiency (Beagle type)

    Pyruvate kinase deficiency of erythrocytes, PK deficiency

  • Pyruvate kinase deficiency (Labrador Retriever type)

    Pyruvate kinase deficiency of erythrocytes, PK deficiency

  • Pyruvate kinase deficiency (Pug type)

    Pyruvate kinase deficiency of erythrocytes, PK deficiency

  • Pyruvate kinase deficiency (Terrier type)

    Erythrocyte pyruvate kinase deficiency, PK Deficiency, PKD

R

  • Renal cystadenocarcinoma and nodular dermatofibrosis

    Renal cancer syndrome

S

  • Sensory ataxic neuropathy

    SAN

  • Severe combined immunodeficiency disease (Terrier type)

    Combined immunodeficiency disease, SCID

  • Severe combined immunodeficiency disease (Wetterhoun type)

    Combined immunodeficiency disease, SCID

  • Severe combined immunodeficiency disease, X-linked (Basset Hound type)

    XSCID

  • Severe combined immunodeficiency disease, X-linked (Corgi type)

    XSCID

  • Skeletal dysplasia 2

    Dwarfism, SD2

  • Spinal dysraphism (Weimaraner type)

  • Spinocerebellar ataxia

    Spinocerebellar ataxia and myokymia, SCA

  • Startle disease

    Hyperekplexia

T

  • Thrombopathia (American Eskimo Dog type)

    Autoimmune thrombocytopenia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Spitz thrombopathia, Thrombocytopathy, Thrombocytopenia

  • Thrombopathia (Basset Hound type)

    Autoimmune thrombocytopenia, Basset Hound thrombopathia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Thrombocytopathy, Thrombocytopenia

  • Thrombopathia (Newfoundland type)

    Autoimmune thrombocytopenia, Hereditary thrombopathy, Immune mediated thrombocytopenia, Platelet disorder, Platelet function defect, Thrombocytopathy, Thrombocytopenia

  • Trapped neutrophil syndrome

    Cohen syndrome, TNS

V

  • Vitamin D dependent rickets, type II (Pomeranian type)

    Hereditary vitamin D-dependent rickets, HVDDR, VDDRII

  • Von Willebrand disease I

    Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 1, von Willebrand's disease, VWDI

  • Von Willebrand disease II

    Pseudohemophilia, Vascular hemophilia, von Willebrand's disease, VWDII

  • Von Willebrand disease III (Kooikerhondje type)

    Pseudohemophilia, Vascular hemophilia, von Willebrand's disease, VWDIII

  • Von Willebrand disease III (Scottish Terrier type)

    Pseudohemophilia, Vascular hemophilia, von Willebrand disease type 3, von Willebrand's disease, VWDIII