Category | Gene(s) | Diseases & coat colors & body characteristics | Malattie & colori del pelo & caratteristiche del corpo (IN ITALIANO) | Abk. / Abb. | V2.1 | V3.0 |
---|---|---|---|---|---|---|
Disease | L2HGDH | L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type) | Aciduria L-2-idrossiglutarica (tipo Staffordshire Bull Terrier) | L-2-HGA | x | x |
Disease | MLKN1 | Lethal Acrodermatitis | Acrodermatite letale | LAD | x | |
Disease | SLC45A2 | Oculocutaneous Albinism | Albinismo oculocutaneo | OCA | x | |
Disease | SLC45A2 | Oculocutaneous Albinism (Small Breed Type) | Albinismo oculocutaneo (tipo di razza piccola) | OCA | x | |
Disease | ENAM | Amelogenesis Imperfecta | Amelogenesi imperfetta | AI | x | x |
Disease | NHEJ1 | Collie Eye Anomaly | Anomalia dell’occhio del Collie | CEA | x | x |
Disease | MYH9 | May-Hegglin Anomaly | Anomalia di May-Hegglin | MHA | x | x |
Disease | CAPN1 | Late Onset Ataxia | Atassia ad esordio tardivo | LOA/SCA | x | x |
Disease | SEL1L | Cerebellar Ataxia (Finnish Hound Type) | Atassia cerebellare (tipo Segugio finlandese) | x | x | |
Disease | KCNJ10 | Spinocerebellar Ataxia | Atassia spinocerebellare | SCA | x | x |
Disease | SAG | Progressive Retinal Atrophy (Basenji Type) | Atrofia progressiva della retina (tipo Basenji) | Basenji-PRA | x | x |
Disease | RHO | Progressive Retinal Atrophy (Bullmastiff/Mastiff Type) | Atrofia progressiva della retina (tipo Bullmastiff/Mastino) | PRA-D | x | x |
Disease | PDE6B | Progressive Retinal Atrophy (Irish Setter Type) | Atrofia progressiva della retina (tipo Setter irlandese) | PRA-rcd1 | x | x |
Disease | CNGA1 | Progressive Retinal Atrophy (Shetland Sheepdog Type) | Atrofia progressiva della retina (tipo Shetland Sheepdog) | CNGA1-PRA | x | |
Disease | PRCD | Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration (prcd) | Atrofia progressiva della retina, degenerazione progressiva del cono-bastoncello (prcd) | PRA-PRCD | x | x |
Disease | NPHP4 | Progressive Retinal Atrophy, Cone-Rod Dystrophy | Atrofia progressiva della retina, distrofia dei coni e dei bastoncelli | PRA-crd / PRA-SWD | x | x |
Disease | SLC4A3 | Progressive Retinal Atrophy, Golden Retriever 1 | Atrofia progressiva della retina, Golden Retriever 1 | GR-PRA1 | x | x |
Disease | TTC8 | Progressive Retinal Atrophy, Golden Retriever 2 | Atrofia progressiva della retina, Golden Retriever 2 | GR-PRA2 | x | x |
Disease | FAM161A | Progressive Retinal Atrophy, PRA3 (Tibetan Terrier and Spaniel Type) | Atrofia progressiva della retina, PRA3 (Tibetan Terrier e Spaniel) | PRA3 | x | |
Disease | NECAP1 | Progressive Retinal Atrophy (Giant Schnauzer Type) | Atrofia retinica progressiva (tipo Schnauzer gigante) | PRA5 | x | |
Disease | PDE6B | Progressive Retinal Atrophy (Sloughi Type) | Atrofia retinica progressiva (tipo Sloughi) | PRA-rcd1a | x | x |
Disease | PDE6A | Progressive Retinal Atrophy, Rod-Cone Dysplasia 3 | Atrofia retinica progressiva, displasia cono-bastoncello 3 | PRA-rcd3 | x | x |
Disease | C2ORF71 | Progressive Retinal Atrophy, Rod-Cone Dysplasia 4 | Atrofia retinica progressiva, displasia cono-bastoncello 4 | PRA-rcd4 | x | |
Disease | PDE6B | Progressive Retinal Atrophy, Cone-Rod Dystrophy 1 | Atrofia retinica progressiva, distrofia cono-bastoncello 1 | PRA-crd1 | x | x |
Disease | IQCB1 | Progressive Retinal Atrophy, Cone-Rod Dystrophy 2 | Atrofia retinica progressiva, distrofia cono-bastoncello 2 | PRA-crd2 | x | |
Disease | ADAM9 | Progressive Retinal Atrophy, Cone-Rod Dystrophy 3 | Atrofia retinica progressiva, distrofia cono-bastoncello 3 | PRA-crd3 | x | x |
Disease | RPGRIP1 | Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 (crd4/cord1) | Atrofia retinica progressiva, distrofia cono-bastoncello 4 (crd4/cord1) | PRA-crd4/cord1 | x | |
Disease | CCDC66 | Progressive Retinal Atrophy, Generalized | Atrofia retinica progressiva, generalizzata | GPRA | x | x |
Disease | RPGR | Progressive Retinal Atrophy, X-Linked 1 | Atrofia retinica progressiva, legata all’X 1 | XLPRA | x | |
Disease | CNGB1 | Progressive Retinal Atrophy, PRA1 (Papillon Type) | Atrofia retinica progressiva, PRA1 (tipo Papillon) | PAP-PRA1 | x | x |
Morphology | BMP3 | Brachycephaly | Brachicefalia | x | x | |
Disease | PDK4 | Dilated Cardiomyopathy (Doberman Pinscher Typ Risk Factor, Variant 1) | Cardiomiopatia dilatativa (fattore di rischio tipo Doberman Pinscher, variante 1) | DCM | x | x |
Disease | TTN | Dilated Cardiomyopathy (Doberman Pinscher Typ Risk Factor, Variant 2) | Cardiomiopatia dilatativa (fattore di rischio tipo Doberman Pinscher, variante 2) | DCM | x | |
Disease | RBM20 | Dilated Cardiomyopathy (Schnauzer Type) | Cardiomiopatia dilatativa (tipo Schnauzer) | DCM | x | |
Disease | C3 | Complement 3 Deficiency | Carenza Complemento 3 | x | x | |
Disease | ITGB2 | Leukocyte Adhesion Deficiency, Type I | Carenza di adesione leucocitaria, tipo I | CLAD-I | x | x |
Disease | FERMT3 | Leukocyte Adhesion Deficiency, Type III | Carenza di adesione leucocitaria, tipo III | CLAD-III | x | x |
Disease | CAT | Catalase Deficiency | Carenza di catalasi | x | ||
Disease | F11 | Factor XI Deficiency | Carenza di fattore XI | x | ||
Disease | MSTN | Myostatin Deficiency (Whippet and Longhaired Whippet Type) | Carenza di miostatina (tipo Whippet e Whippet a pelo lungo) | x | x | |
Disease | PKLR | Pyruvate Kinase Deficiency (Basenji Type) | Carenza di piruvato chinasi (tipo Basenji) | PKDef | x | x |
Disease | PKLR | Pyruvate Kinase Deficiency (Beagle Type) | Carenza di piruvato chinasi (tipo Beagle) | PKDef | x | x |
Disease | PKLR | Pyruvate Kinase Deficiency (Pug Type) | Carenza di piruvato chinasi (tipo Carlino) | PKDef | x | x |
Disease | PKLR | Pyruvate Kinase Deficiency (Labrador Retriever Type) | Carenza di piruvato chinasi (tipo Labrador Retriever) | PKDef | x | x |
Disease | PKLR | Pyruvate Kinase Deficiency (Terrier Type) | Carenza di piruvato chinasi (tipo Terrier) | PKDef | x | x |
Disease | PDP1 | Pyruvate Dehydrogenase Deficiency | Carenza di piruvato deidrogenasi | PDH | x | x |
Disease | HSF4 | Hereditary Cataracts | Cataratta ereditaria | HC1 | x | x |
Disease | HSF4 | Hereditary Cataracts (Australian Shepherd Type) | Cataratta ereditaria (tipo Pastore australiano) | HC2 | x | x |
Disease | RPE65 | Congenital Stationary Night Blindness | Cecità congenita notturna stazionaria | CSNB | x | x |
Disease | ATP13A2 | Neuronal Ceroid Lipofuscinosis (Tibetan Terrier Type) | Ceroidolipofuscinosi neuronale (tipo Terrier tibetano) | NCL-A | x | x |
Disease | PPT1 | Neuronal Ceroid Lipofuscinosis 1 | Ceroidolipofuscinosi neuronale 1 | NCL-1 | x | x |
Disease | PPT1 | Neuronal Ceroid Lipofuscinosis 1 (Cane Corso Type) | Ceroidolipofuscinosi neuronale 1 (tipo Cane Corso) | NCL-1 | x | x |
Disease | CTSD | Neuronal Ceroid Lipofuscinosis 10 | Ceroidolipofuscinosi neuronale 10 | NCL-10 | x | x |
Disease | ATP13A2 | Neuronal Ceroid Lipofuscinosis 12 | Ceroidolipofuscinosi neuronale 12 | NCL-12 | x | |
Disease | TPP1 | Neuronal Ceroid Lipofuscinosis 2 | Ceroidolipofuscinosi neuronale 2 | NCL-2 | x | x |
Disease | ARSG | Neuronal Ceroid Lipofuscinosis 4A | Ceroidolipofuscinosi neuronale 4A | NCLA-4A | x | x |
Disease | CLN5 | Neuronal Ceroid Lipofuscinosis 5 (Australian Cattle Dog/Border Collie Type) | Ceroidolipofuscinosi neuronale 5 (tipo Australian Cattle Dog/Border Collie) | NCL-5 | x | x |
Disease | CLN5 | Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type) | Ceroidolipofuscinosi neuronale 5 (tipo Golden Retriever) | NCL-5 | x | |
Disease | CLN6 | Neuronal Ceroid Lipofuscinosis 6 | Ceroidolipofuscinosi neuronale 6 | NCL-6 | x | x |
Disease | MFSD8 | Neuronal Ceroid Lipofuscinosis 7 | Ceroidolipofuscinosi neuronale 7 | NCL-7 | x | |
Disease | CLN8 | Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type) | Ceroidolipofuscinosi neuronale 8 (tipo Pastore australiano) | NCL-8 | x | x |
Disease | CLN8 | Neuronal Ceroid Lipofuscinosis 8 (Setter Type) | Ceroidolipofuscinosi neuronale 8 (tipo Setter) | NCL-8 | x | x |
Disease | SLC3A1 | Cystinuria (Australian Cattle Dog typ) | Cistinuria (tipo Australian Cattle Dog) | x | x | |
Disease | SLC3A1 | Cystinuria (Labrador Retriever Typ) | Cistinuria (tipo Labrador Retriever) | x | x | |
Disease | SLC7A9 | Cystinuria (Miniature Pinscher Typ) | Cistinuria (tipo Pinscher in miniatura) | x | x | |
Disease | SLC3A1 | Cystinuria (Newfoundland Typ) | Cistinuria (tipo Terranova) | x | x | |
Disease | SLC7A9 | Cystinuria Typ 3 (Bulldog Typ Risk Factor, Variant 3) | Cistinuria tipo 3 (fattore di rischio tipo Bulldog, variante 3) | x | ||
Disease | SLC3A1 | Cystinuria Typ 3 (Bulldog Typ Risk Factor, Variants 1 and 2) | Cistinuria tipo 3 (fattore di rischio tipo Bulldog, varianti 1 e 2) | x | ||
Disease | FLCN | Renal Cystadenocarcinoma and Nodular Dermatofibrosis | Cistodenocarcinoma renale e dermatofibrosi nodulare | RCND | x | x |
Disease | DNM1 | Exercise-Induced Collapse | Collasso indotto dall’esercizio | EIC | x | x |
Morphology | FGF4 | Chondrodysplasia | Condrodisplasia | x | x | |
Disease | ITGA10 | Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound Type) | Condrodisplasia (Cane Orso Careliano e Tipo Elkhound Norvegese) | x | x | |
Disease | F7 | Coagulation Factor VII Deficiency | Deficit del fattore VII della coagulazione | x | x | |
Disease | KLKB1 | Prekallikrein Deficiency | Deficit di precallicreina | x | x | |
Disease | RAB24 | Cerebellar Degeneration | Degenerazione cerebellare | x | ||
Disease | SNX14 | Cerebellar Cortical Degeneration | Degenerazione corticale cerebellare | CCD | x | |
Disease | SPTBN2 | Neonatal Cerebellar Cortical Degeneration | Degenerazione corticale cerebellare neonatale | NCCD | x | x |
Disease | CNGB3 | Cone Degeneration | Degenerazione del cono | CD | x | x |
Disease | CNGA3 | Cone Degeneration (Labrador Retriever Type) | Degenerazione del cono (tipo Labrador Retriever) | CD | x | |
Disease | CNGA3 | Cone Degeneration (German Shepherd Dog Type) | Degenerazione del cono (tipo Pastore tedesco) | CD | x | |
Disease | CNGB3 | Cone Degeneration (German Shorthaired Pointer Type) | Degenerazione del cono (tipo Puntatore tedesco a pelo corto) | CD | x | x |
Disease | SERAC1 | Canine Multiple System Degeneration (Chinese Crested Type) | Degenerazione multisistemica canina (Tipo Cinese Crestato) | CMSD | x | x |
Disease | SERAC1 | Canine Multiple System Degeneration (Kerry Blue Terrier Type) | Degenerazione multisistemica canina (Tipo Kerry Blue Terrier) | CMSD | x | x |
Disease | STK38L | Early Retinal Degeneration | Degenerazione retinica precoce | ERD | x | x |
Coat color | AMELXY | Sex Determination – X | Determinazione del sesso – X | x | x | |
Coat color | ZFXY | Sex Determination – Y | Determinazione del sesso – Y | x | x | |
Disease | CCDC39 | Primary Ciliary Dyskinesia | Discinesia ciliare primaria | PCD | x | x |
Disease | PIGN | Adult Paroxysmal Dyskinesia | Discinesia parossistica dell’adulto | PxD | x | |
Disease | HES7 | Spondylocostal Dysostosis | Disostosi spondilocostale | SCD | x | |
Disease | PKP1 | Ectodermal Dysplasia (Chesapeake Bay Retriever Type) | Displasia ectodermica (tipo Chesapeake Bay Retriever) | ED | x | x |
Disease | EDA | Ectodermal Dysplasia, X-Linked (Dachshund Type) | Displasia ectodermica, legata all’X (tipo Bassotto) | XED | x | |
Disease | EDA | Ectodermal Dysplasia, X-Linked (Shepherd Type) | Displasia ectodermica, legata all’X (tipo Pastore) | XED | x | x |
Disease | INPP5E | Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis | Displasia renale cistica diffusa e fibrosi epatica | x | ||
Disease | COL9A3 | Retinal Dysplasia/Oculoskeletal Dysplasia 1 | Displasia retinica/displasia oculoscheletrica 1 | RD/OSD1 | x | |
Disease | COL9A2 | Retinal Dysplasia/Oculoskeletal Dysplasia 2 | Displasia retinica/displasia oculoscheletrica 2 | RD/OSD2 | x | |
Disease | COL11A2 | Skeletal Dysplasia 2 | Displasia scheletrica 2 | SD2 | x | x |
Disease | NKX2-8 | Spinal Dysraphism | Disrafismo spinale | x | x | |
Disease | CHST6 | Macular Corneal Dystrophy (Labrador Retriever Type) | Distrofia corneale maculare (tipo Labrador Retriever) | MD | x | |
Disease | DMD | Muscular Dystrophy (Golden Retriever Type) | Distrofia muscolare (tipo Golden Retriever) | GRMD | x | x |
Disease | DMD | Pembroke Welsh Corgi Duchenne Muscular Dystrophy | Distrofia muscolare di Duchenne per Pembroke Welsh Corgi | DMD | x | x |
Disease | TECPR2 | Neuroaxonal Dystrophy (Spanish Water Dog Type) | Distrofia neuroassonale (tipo Cane da acqua spagnolo) | NAD | x | |
Disease | VPS11 | Neuroaxonal Dystrophy (Rottweiler Type) | Distrofia neuroassonale (tipo Rottweiler) | NAD | x | |
Disease | ATG4D | Lagotto Storage Disorder | Disturbo da accumulo del Lagotto | LSD | x | |
Disease | P2RY12 | P2RY12 Receptor Platelet Disorder | Disturbo piastrinico del recettore P2RY12 | x | x | |
Disease | SPTB | Elliptocytosis | Ellistocitosi | x | x | |
Disease | F8 | Hemophilia A (German Shepherd Dog, Type 1) | Emofilia A (pastore tedesco, tipo 1) | HämA | x | x |
Disease | F8 | Hemophilia A (German Shepherd Dog, Type 2) | Emofilia A (pastore tedesco, tipo 2) | HämA | x | x |
Disease | F8 | Hemophilia A (Boxer Type) | Emofilia A (tipo Boxer) | HämA | x | x |
Disease | F9 | Hemophilia B (Cairn Terrier Type) | Emofilia B (tipo Cairn Terrier) | HämB | x | x |
Disease | F9 | Hemophilia B (Lhasa Apso Type) | Emofilia B (tipo Lhasa Apso) | HämB | x | x |
Disease | F9 | Hemophilia B (Rhodesian Ridgeback Type) | Emofilia B (tipo Rhodesian Ridgeback) | HämB | x | x |
Disease | SLC19A3 | Alaskan Husky Encephalopathy | Encefalopatia dell’Husky Alaskano | AHE | x | x |
Disease | ATF2 | Neonatal Encephalopathy with Seizures | Encefalopatia neonatale con convulsioni | NEWS | x | x |
Disease | COL7A1 | Dystrophic Epidermolysis Bullosa | Epidermolisi bollosa distrofica | DEB | x | x |
Disease | LGI2 | Benign Familial Juvenile Epilepsy | Epilessia giovanile familiare benigna | BFJE | x | x |
Disease | DIRAS1 | Juvenile Myoclonic Epilepsy (Rhodesian Ridgeback Type) | Epilessia mioclonica giovanile (tipo Rhodesian Ridgeback) | JME | x | x |
Disease | FUCA1 | Fucosidosis | Fucosidosi | FUC | x | |
Disease | GLB1 | GM1 Gangliosidosis (Portuguese Water Dog Type) | Gangliosidosi GM1 (tipo Cane da acqua portoghese) | GM1 | x | x |
Disease | GLB1 | GM1 Gangliosidosis (Alaskan Husky Type) | Gangliosidosi GM1 (tipo Husky Alaskano) | GM1 | x | x |
Disease | GLB1 | GM1 Gangliosidosis (Shiba Inu Type) | Gangliosidosi GM1 (tipo Shiba Inu) | GM1 | x | x |
Disease | HEXB | GM2 Gangliosidosis (Poodle Type) | Gangliosidosi GM2 (tipo Barboncino) | GM2 | x | x |
Disease | HEXA | GM2 Gangliosidosis (Japanese Chin Type) | Gangliosidosi GM2 (tipo Chin giapponese) | GM2 | x | x |
Disease | OLFML3 | Glaucoma (Border Collie Type) | Glaucoma (tipo Border Collie) | x | ||
Disease | ADAMTS10 | Primary Open Angle Glaucoma | Glaucoma primario ad angolo aperto | POAG | x | x |
Disease | ADAMTS17 | Primary Open Angle Glaucoma (Basset Fauve de Bretagne Type) | Glaucoma primario ad angolo aperto (tipo Basset Fauve de Bretagne) | POAG | x | |
Disease | ADAMTS17 | Primary Open Angle Glaucoma (Basset Hound Type) | Glaucoma primario ad angolo aperto (tipo Basset Hound) | POAG | x | |
Disease | ADAMTS10 | Primary Open Angle Glaucoma (Norwegian Elkhound Type) | Glaucoma primario ad angolo aperto (tipo Elkhound norvegese) | POAG | x | |
Disease | ADAMTS17 | Primary Open Angle Glaucoma and Primary Lens Luxation (Shar Pei Type) | Glaucoma primario ad angolo aperto e lussazione primaria del cristallino (tipo Shar Pei) | POAG/PLL | x | |
Disease | KRT10 | Epidermolytic Hyperkeratosis | Ipercheratosi epidermolitica | x | x | |
Disease | FAM83G | Hereditary Footpad Hyperkeratosis (Irish Terrier and Kromfohrländer Type) | Ipercheratosi ereditaria del cuscinetto plantare (tipo Irish Terrier e Kromfohrländer) | HFH | x | x |
Disease | AGXT | Primary Hyperoxaluria | Iperossaluria primaria | PH1 | x | x |
Disease | SLC2A9 | Hyperuricosuria | Iperuricosuria | HUU | x | x |
Disease | FNIP2 | Hypomyelination (Weimaraner Type) | Ipomielinizzazione (tipo Weimaraner) | x | ||
Disease | FAM20C | Dental Hypomineralization | Ipomineralizzazione dentale | x | ||
Disease | TPO | Congenital Hypothyroidism with Goiter (Terrier Type) | Ipotiroidismo congenito con gozzo (tipo Terrier) | x | ||
Disease | SLC27A4 | Ichthyosis (Great Dane Type) | Ittiosi (tipo Alano) | x | ||
Disease | NIPAL4 | Ichthyosis (American Bulldog Type) | Ittiosi (tipo Bulldog americano) | x | x | |
Disease | PNPLA1 | Ichthyosis (Golden Retriever Type) | Ittiosi (tipo Golden Retriever) | x | x | |
Disease | GALC | Globoid Cell Leukodystrophy (Irish Setter Type) | Leucodistrofia a cellule globoidi (tipo Setter irlandese) | GLD | x | x |
Disease | GALC | Globoid Cell Leukodystrophy (Terrier Type) | Leucodistrofia a cellule globoidi (tipo Terrier) | GLD | x | x |
Coat color | ASIP | A Locus (Agouti) – a^w/a^t | Locus A ( (Agouti) – a^w/a^t | x | x | |
Coat color | ASIP | A Locus (Agouti) – a | Locus A ( (Agouti) – a | x | x | |
Coat color | ASIP | A Locus (Agouti) – a A Locus (Agouti) – A^y | Locus A (Agouti) – a A Locus (Agouti) – A^y | x | x | |
Coat color | RALY | As Locus (Saddle Tan) | Locus As (Saddle Tan) | x | ||
Coat color | TYRP1 | B Locus (Brown) – b^a | Locus B (marrone) – b^a | x | x | |
Coat color | TYRP1 | B Locus (Brown) – b^c | Locus B (marrone) – b^c | x | x | |
Coat color | TYRP1 | B Locus (Brown) – b^d | Locus B (marrone) – b^d | x | x | |
Coat color | TYRP1 | B Locus (Brown) – b^s | Locus B (marrone) – b^s | x | x | |
Coat Texture | KRT71 | Cu Locus (Curly Hair) | Locus Cu (capelli ricci) | x | x | |
Coat color | MLPH | D Locus (Dilute) – d^1 | Locus D (diluito) – d^1 | x | x | |
Coat color | MLPH | D Locus (Dilute) – d^2 | Locus D (diluito) – d^2 | x | x | |
Coat color | MC1R | E Locus (Yellow/Red) | Locus E (giallo/rosso) | x | x | |
Coat color | MC1R | Eg Locus (Grizzle, Afghan Hound Type) | Locus Eg (grigio, tipo Levriero Afgano) | x | x | |
Coat color | MC1R | Eh Locus (Sable, Cocker Spaniel Type) | Locus Eh (zibellino, tipo Cocker Spaniel) | x | ||
Coat color | MC1R | Em Locus (Melanistic Mask) | Locus Em (Maschera Melanistica) | x | x | |
Coat color | PSMB7 | H Locus (Harlequin, Great Dane Type) | Locus H (Arlecchino, Alano) | x | x | |
Coat Texture | FOXI3 | Hr Locus (FOXI3 Hairless Gene Test, Mexican Hairless, Peruvian Hairless and Chinese Crested Type) | Locus Hr (test genetico per glabro FOXI3, glabro messicano, glabro peruviano e crestato cinese) | x | ||
Coat color | MFSD12 | I Locus (Intensity) | Locus I (Intensità) | x | ||
Coat color | RSPO2 | IC Locus (Improper Coat/Furnishings) | Locus IC (Rivestimento/pelo improprio) | x | ||
Coat color | CBD103 | K Locus (Dominant Black) | Locus K (nero dominante) | x | x | |
Coat color | FGF5 | L Locus (Long Hair/Fluffy) – Lh^1 | Locus L (capelli lunghi/soffice) – Lh^1 | x | x | |
Coat color | FGF5 | L Locus (Long Hair/Fluffy) – Lh^2 | Locus L (capelli lunghi/soffice) – Lh^2 | x | x | |
Coat color | MITF | S Locus (White Spotting, Parti, or Piebald) | Locus S (macchia bianca, parti o pezzato) | x | ||
Coat color | MC5R | SD Locus (Shedding) | Locus SD (spargimento) | x | x | |
Morphology | T | T Locus (Natural Bobtail) | Locus T (Bobtail naturale) | x | x | |
Coat color | PMEL | M Locus (Merle) | Luogo M (Merle) | x | ||
Disease | ADAMTS17 | Primary Lens Luxation | Lussazione primaria della lente | PLL | x | x |
Disease | CUBN | Intestinal Cobalamin Malabsorption (Beagle Type) | Malassorbimento intestinale di cobalamina (tipo Beagle) | IGS | x | x |
Disease | CUBN | Intestinal Cobalamin Malabsorption (Border Collie Type) | Malassorbimento intestinale di cobalamina (tipo Border Collie) | IGS | x | x |
Disease | MTBP | Shar-Pei Autoinflammatory Disease | Malattia autoinfiammatoria Shar-Pei | SPAID | x | x |
Disease | G6PC | Glycogen Storage Disease Ia | Malattia da accumulo di glicogeno Ia | GSD-Ia | x | x |
Disease | AGL | Glycogen Storage Disease IIIa | Malattia da accumulo di glicogeno IIIa | GSD-IIIa | x | x |
Disease | PFKM | Glycogen Storage Disease VII (Wachtelhund Type) | Malattia da accumulo di glicogeno VII (tipo Wachtelhund) | GSD-VII/PFL | x | x |
Disease | PFKM | Glycogen Storage Disease VII, PFK Deficiency | Malattia da accumulo di glicogeno VII, carenza di PFK | GSD-VII/PFL | x | x |
Disease | PRKDC | Severe Combined Immunodeficiency Disease (Terrier Type) | Malattia da immunodeficienza combinata grave (tipo Terrier) | SCID | x | x |
Disease | RAG1 | Severe Combined Immunodeficiency Disease (Wetterhoun Type) | Malattia da immunodeficienza combinata grave (tipo Wetterhoun) | SCID | x | x |
Disease | IL2RG | Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type) | Malattia da immunodeficienza combinata grave, legata all’X (tipo Basset Hound) | XSCID | x | x |
Disease | IL2RG | Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type) | Malattia da immunodeficienza combinata grave, legata all’X (tipo Corgi) | XSCID | x | x |
Disease | SLC6A5 | Startle Disease | Malattia da sussulto | x | x | |
Disease | FGF4 | Intervertebral Disc Disease and Chondrodystrophy | Malattia del disco intervertebrale e Condrodistrofia | IVDD | x | |
Disease | GAA | Pompe Disease | Malattia di Pompe | GSD-II | x | x |
Disease | ABCA4 | Stargardt Disease | Malattia di Stargardt | STGD | x | |
Disease | VWF | Von Willebrand Disease I | Malattia di Von Willebrand I | VWDI | x | x |
Disease | VWF | Von Willebrand Disease II | Malattia di Von Willebrand II | VWDII | x | x |
Disease | VWF | Von Willebrand Disease III (Kooikerhondje Type) | Malattia di Von Willebrand III (tipo Kooikerhondje) | VWDIII | x | x |
Disease | VWF | Von Willebrand Disease III (Shetland Sheepdog Type) | Malattia di Von Willebrand III (tipo Pastore delle Shetland) | VWDIII | x | x |
Disease | VWF | Von Willebrand Disease III (Scottish Terrier Type) | Malattia di Von Willebrand III (tipo Scottish Terrier) | VWDIII | x | x |
Disease | AKNA | Recurrent Inflammatory Pulmonary Disease | Malattia polmonare infiammatoria ricorrente | IPD | x | |
Disease | VLDLR | Dandy-Walker-Like Malformation | Malformazione Dandy-Walker | x | ||
Disease | PLG | Ligneous Membranitis | Membranite lignea | LM | x | x |
Disease | CYB5R3 | Congenital Methemoglobinemia | Metaemoglobinemia congenita | x | ||
Disease | SOD1 | Degenerative Myelopathy (Bernese Mountain Dog Variant) | Mielopatia degenerativa (variante Bovaro bernese) | DM | x | |
Disease | SOD1 | Degenerative Myelopathy (Common Variant) | Mielopatia degenerativa (variante comune) | DM | x | x |
Disease | PTPLA | Centronuclear Myopathy | Miopatia centronucleare | CNM | x | |
Disease | BIN1 | Inherited Myopathy of Great Danes | Miopatia ereditaria degli Alani | IMGD | x | x |
Disease | MTM1 | Myotubular Myopathy 1 | Miopatia miotubulare 1 | x | x | |
Disease | MTM1 | Myotubular Myopathy 1 (Rottweiler Type) | Miopatia miotubulare 1 (tipo Rottweiler) | x | ||
Disease | CLCN1 | Myotonia Congenita (Australian Cattle Dog Type) | Miotonia congenita (tipo Bovaro Australiano) | MC | x | x |
Disease | CLCN1 | Myotonia Congenita (Schnauzer Type) | Miotonia congenita (tipo Schnauzer) | MC | x | x |
Disease | SP110 | Degenerative Myelopathy Modifier (Pembroke Welsh Corgi Typ) | Modificatore della mielopatia degenerativa (tipo Pembroke Welsh Corgi) | DM | x | x |
Disease | ABCB4 | Gallbladder Mucoceles | Mucocele della cistifellea | x | x | |
Disease | IDUA | Mucopolysaccharidosis I | Mucopolisaccaridosi I | MPS-I | x | x |
Disease | SGSH | Mucopolysaccharidosis IIIA (Dachshund Type) | Mucopolisaccaridosi IIIA (tipo Bassotto) | MPS-IIIA | x | x |
Disease | SGSH | Mucopolysaccharidosis IIIA (New Zealand Huntaway Type) | Mucopolisaccaridosi IIIA (tipo New Zealand Huntaway) | MPS-IIIA | x | x |
Disease | GUSB | Mucopolysaccharidosis VII (Shepherd Type) | Mucopolisaccaridosi VII (tipo Pastore) | MPS-VII | x | x |
Disease | ABCB1 | Multidrug Resistance 1 | Multiresistenza ai farmaci 1 | MDR1 | x | x |
Disease | HCRTR2 | Narcolepsy (Dachshund Type) | Narcolessia (tipo Bassotto) | NARC | x | x |
Disease | HCRTR2 | Narcolepsy (Doberman Pinscher Type) | Narcolessia (tipo Doberman Pinscher) | NARC | x | x |
Disease | HCRTR2 | Narcolepsy (Labrador Retriever Type) | Narcolessia (tipo Labrador Retriever) | NARC | x | x |
Disease | COL4A5 | Hereditary Nephritis (Samoyed Type) | Nefrite ereditaria (tipo Samoiedo) | XLHN | x | x |
Disease | KIRREL2 | Protein Losing Nephropathy – Variant 1 | Nefropatia con perdita di proteine - Variante 1 | PLN-1 | x | |
Disease | NPHS1 | Protein Losing Nephropathy – Variant 2 | Nefropatia con perdita di proteine - Variante 2 | PLN-2 | x | |
Disease | COL4A4 | Familial Nephropathy (Cocker Spaniel Type) | Nefropatia familiare (tipo Cocker Spaniel) | FN | x | x |
Disease | COL4A4 | Familial Nephropathy (English Springer Spaniel Type) | Nefropatia familiare (tipo Springer Spaniel inglese) | FN | x | x |
Disease | FAM134B | Sensory Neuropathy (Border Collie Type) | Neuropatia sensoriale (tipo Border Collie) | SN | x | |
Disease | AP3B1 | Cyclic Neutropenia | Neutropenia ciclica | CN | x | x |
Disease | SLC13A1 | Osteochondrodysplasia | Osteocondrodisplasia | OCD | x | |
Disease | SERPINH1 | Osteogenesis Imperfecta (Dachshund Type) | Osteogenesi imperfetta (tipo Bassotto) | OI | x | x |
Disease | COL1A2 | Osteogenesis Imperfecta (Beagle Type) | Osteogenesi imperfetta (tipo Beagle) | OI | x | x |
Disease | COL1A1 | Osteogenesis Imperfecta (Golden Retriever Type) | Osteogenesi imperfetta (tipo Golden Retriever) | OI | x | x |
Disease | SLC37A2 | Craniomandibular Osteopathy | Osteopatia craniomandibolare | CMO | x | |
Disease | ADAMTS20 | Cleft Palate and Syndactyly (Nova Scotia Duck Tolling Retriever Type) | Palatoschisi e sindattilia (tipo Nova Scotia Duck Tolling Retriever) | x | ||
Disease | SUV39H2 | Hereditary Nasal Parakeratosis | Paracheratosi nasale ereditaria | HNPK | x | x |
Disease | SUV39H2 | Hereditary Nasal Parakeratosis (Greyhound Type) | Paracheratosi nasale ereditaria (tipo Greyhound) | HNPK | x | |
Disease | RAB3GAP1 | Juvenile Laryngeal Paralysis and Polyneuropathy | Paralisi laringea giovanile e polineuropatia | x | x | |
Morphology | LMBR1 | Polydactyly | Polidattilia | x | x | |
Disease | GJA9 | Polyneuropathy (Leonberger Type 2) | Polineuropatia (Leonberger Tipo 2) | LPN2 | x | x |
Disease | ARHGEF10 | Polyneuropathy (Leonberger and Saint Bernard Type) | Polineuropatia (tipo Leonberger e San Bernardo) | LPN1 | x | x |
Disease | RAB3GAP1 | Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation | Polineuropatia con anomalie oculari e vacuolizzazione neuronale | POAVN | x | |
Disease | NDRG1 | Greyhound Polyneuropathy | Polineuropatia da Levriero | x | x | |
Disease | NDRG1 | Alaskan Malamute Polyneuropathy | Polineuropatia del Malamute Alaskano | AMPN | x | x |
Disease | BEST1 | Multifocal Retinopathy 1 | Retinopatia multifocale 1 | CMR1 | x | x |
Disease | BEST1 | Multifocal Retinopathy 2 | Retinopatia multifocale 2 | CMR2 | x | x |
Disease | BEST1 | Multifocal Retinopathy 3 | Retinopatia multifocale 3 | CMR3 | x | x |
Disease | ANO6 | Canine Scott Syndrome | Sindrome canina di Scott | CSS | x | |
Disease | BCAN | Episodic Falling Syndrome | Sindrome da caduta episodica | EFS | x | x |
Disease | GDNF | Acral Mutilation Syndrome | Sindrome da mutilazione acrale | AMS | x | |
Disease | VPS13B | Trapped Neutrophil Syndrome | Sindrome da neutrofili intrappolati | TNS | x | x |
Disease | ANLN | Acute Respiratory Distress Syndrome | Sindrome da pena respiratoria acuta | ARDS | x | |
Disease | AMHR2 | Persistent Müllerian Duct Syndrome | Sindrome del dotto mulleriano persistente | PMS | x | x |
Disease | FAM83H | Dry Eye Curly Coat Syndrome | Sindrome del pelo riccio dell’occhio secco | CKSID | x | x |
Disease | TNXB | Ehlers-Danlos Syndrome (Variant 1) | Sindrome di Ehlers-Danlos (variante 1) | EDS | x | |
Disease | TNXB | Ehlers-Danlos Syndrome (Variant 2) | Sindrome di Ehlers-Danlos (variante 2) | EDS | x | |
Disease | LEPREL1 | Lundehund Syndrome | Sindrome di Lundehund | x | ||
Disease | ADAMTSL2 | Musladin-Lueke Syndrome | Sindrome di Musladin-Lueke | MLS | x | x |
Disease | SCARF2 | Van Den Ende-Gupta Syndrome | Sindrome di Van Den Ende-Gupta | VDEGS | x | |
Disease | CHAT | Congenital Myasthenic Syndrome (Old Danish Pointer Type) | Sindrome miastenica congenita (tipo di puntatore danese antico) | CMS | x | x |
Disease | CHRNE | Congenital Myasthenic Syndrome (Jack Russell Terrier Type) | Sindrome miastenica congenita (tipo Jack Russell Terrier) | CMS | x | |
Disease | COLQ | Congenital Myasthenic Syndrome (Labrador Retriever Type) | Sindrome miastenica congenita (tipo Labrador Retriever) | CMS | x | x |
Disease | ITGA2B | Glanzmann’s Thrombasthenia (Great Pyrenees Type) | Trombastenia di Glanzmann (tipo dei Grandi Pirenei) | GT | x | x |
Disease | ITGA2B | Glanzmann’s Thrombasthenia (Otterhound Type) | Trombastenia di Glanzmann (tipo Otterhound) | GT | x | x |
Disease | RASGRP1 | Thrombopathia (Basset Hound Type) | Trombopatia (tipo Basset Hound) | x | x | |
Disease | RASGRP1 | Thrombopathia (American Eskimo Dog Type) | Trombopatia (tipo Eschimese americano) | x | x | |
Disease | RASGRP1 | Thrombopathia (Newfoundland Type) | Trombopatia (tipo Terranova) | x | x | |
Disease | APRT | Urolithiasis (Native American Indian Dog Type) | Urolitiasi (tipo Cane indiano nativo americano) | x |