Category |
Diseases & coat colors & body characteristics |
Malattie & colori del pelo & caratteristiche del corpo (IN ITALIANO) |
Diseases |
Spinal Muscular Atrophy |
Atrofia muscolare spinale |
Diseases |
Progressive Retinal Atrophy (Abyssinian Type) |
Atrofia progressiva della retina (tipo abissino) |
Diseases |
Progressive Retinal Atrophy (Persian Type) |
Atrofia progressiva della retina (tipo persiano) |
Coat Colour |
Dominant White, White Spotting and Gloves – W Locus |
Bianco dominante, macchie bianche e guanti – Locus W |
Diseases |
Brachycephaly (Burmese Type) |
Brachicefalia (tipo birmano) |
Trait |
Long Hair – L Locus |
Capelli lunghi – Locus L |
Trait |
Curly Coat (Cornish Rex Type) |
Pelo riccio (tipo Cornish Rex) |
Diseases |
Hypertrophic Cardiomyopathy (Maine Coon Type) |
Cardiomiopatia ipertrofica (tipo Maine Coon) |
Diseases |
Hypertrophic Cardiomyopathy (Ragdoll Type) |
Cardiomiopatia ipertrofica (tipo Ragdoll) |
Diseases |
Factor XII Deficiency, Variant 1 |
Carenza di fattore XII, variante 1 |
Diseases |
Pyruvate Kinase Deficiency |
Carenza di piruvato chinasi |
Diseases |
Cystinuria, Type 1A |
Cistinuria, tipo 1A |
Diseases |
Cystinuria, Type B, Variant 1 |
Cistinuria, tipo B, variante 1 |
Diseases |
Cystinuria, Type B, Variant 2 |
Cistinuria, tipo B, variante 2 |
Diseases |
Cystinuria, Type B, Variant 3 |
Cistinuria, tipo B, variante 3 |
Diseases |
Cystinuria, Type B, Variant 4 |
Cistinuria, tipo B, variante 4 |
Diseases |
Cystinuria, Type B, Variant 5 |
Cistinuria, tipo B, variante 5 |
Trait |
Short Tail (Japanese Bobtail Type) |
Coda corta (tipo Bobtail giapponese) |
Coat Colour |
Pointed Coat Color and Albinism – C Locus |
Colore del pelo a punta e albinismo – Locus C |
Coat Colour |
Agouti Coat Color – A Locus |
Colore del pelo agouti: un locus |
Coat Colour |
Amber and Russet Coat Color – E Locus |
Colore del pelo ambra e ruggine – Locus E |
Coat Colour |
Dilute Coat Color – D Locus |
Colore del pelo diluito – Locus D |
Coat Colour |
Brown Coat Color – B Locus |
Colore del pelo marrone – Locus B |
Diseases |
Feline Leukocyte Adhesion Deficiency, Type 1 |
Deficit di adesione leucocitaria felina, tipo 1 |
Diseases |
Dihydropyrimidinase Deficiency |
Deficit di diidropirimidinasi |
Diseases |
Hemophilia B, Variant 1 |
Emofilia B, variante 1 |
Diseases |
Hemophilia B, Variant 2 |
Emofilia B, variante 2 |
Diseases |
GM1 Gangliosidosis |
Gangliosidosi GM1 |
Diseases |
GM2 Gangliosidosis, Type II |
Gangliosidosi GM2, tipo II |
Diseases |
GM2 Gangliosidosis, Type II (Burmese Type) |
Gangliosidosi GM2, tipo II (tipo birmano) |
Diseases |
GM2 Gangliosidosis, Type II (Japanese Domestic Type) |
Gangliosidosi GM2, tipo II (tipo domestico giapponese) |
Diseases |
GM2 Gangliosidosis, Type II (Korat Type) |
Gangliosidosi GM2, tipo II (tipo Korat) |
Diseases |
Gangliosidosis GM2A |
Gangliosidosi GM2A |
Diseases |
Hyperlipoproteinemia |
Iperlipoproteinemia |
Diseases |
Primary Hyperoxaluria Type II |
Iperossaluria primaria di tipo II |
Diseases |
Congenital Adrenal Hyperplasia |
Iperplasia surrenale congenita |
Diseases |
Congenital Hypothyroidism |
Ipotiroidismo congenito |
Diseases |
Hypotrichosis with Short Life Expectancy |
Ipotricosi con aspettativa di vita breve |
Diseases |
Glycogen Storage Disease, Type IV |
Malattia da accumulo di glicogeno, tipo IV |
Diseases |
Niemann-Pick C1 Disease, Variant 1 |
Malattia di Niemann-Pick C1, variante 1 |
Diseases |
Niemann-Pick C1 Disease, Variant 2 |
Malattia di Niemann-Pick C1, variante 2 |
Diseases |
Niemann-Pick C2 Disease |
Malattia di Niemann-Pick C2 |
Diseases |
Polycystic Kidney Disease |
Malattia policistica renale |
Diseases |
Myotonia Congenita |
Miotonia congenita |
Coat Colour |
Tabby Coat Color Pattern – Mc Locus |
Modello di colore del pelo tabby – Locus Mc |
Diseases |
Mucopolysaccharidosis Type I |
Mucopolisaccaridosi di tipo I |
Diseases |
Mucopolysaccharidosis Type VI (Mild Form) |
Mucopolisaccaridosi di tipo VI (forma lieve) |
Diseases |
Mucopolysaccharidosis Type VI (Siamese Type) |
Mucopolisaccaridosi di tipo VI (tipo siamese) |
Diseases |
Mucopolysaccharidosis Type VII, Variant 1 |
Mucopolisaccaridosi di tipo VII, variante 1 |
Diseases |
Mucopolysaccharidosis Type VII, Variant 2 |
Mucopolisaccaridosi di tipo VII, variante 2 |
Trait |
Folded Ears with Osteochondrodysplasia |
Orecchie piegate con osteocondrodisplasia |
Diseases |
Hypokalemic Periodic Paralysis |
Paralisi periodica ipokaliemica |
Trait |
Polydactyly |
Polidattilia |
Diseases |
Acute Intermittent Porphyria, Variant 1 |
Porfiria acuta intermittente, variante 1 |
Diseases |
Acute Intermittent Porphyria, Variant 2 |
Porfiria acuta intermittente, variante 2 |
Diseases |
Acute Intermittent Porphyria, Variant 3 |
Porfiria acuta intermittente, variante 3 |
Diseases |
Acute Intermittent Porphyria, Variant 4 (Siamese Type 1) |
Porfiria acuta intermittente, variante 4 (siamese di tipo 1) |
Diseases |
Acute Intermittent Porphyria, Variant 5 (Siamese Type 2) |
Porfiria acuta intermittente, variante 5 (siamese di tipo 2) |
Diseases |
Acute Intermittent Porphyria, Variant 6 |
Porfiria acuta intermittente, variante 6 |
Diseases |
Congenital Erythropoietic Porphyria, Variant 1 |
Porfiria eritropoietica congenita, variante 1 |
Diseases |
Congenital Erythropoietic Porphyria, Variant 2 |
Porfiria eritropoietica congenita, variante 2 |
Diseases |
Vitamin D-dependent Rickets, Type IA, Variant 1 |
Rachitismo dipendente dalla vitamina D, tipo IA, variante 1 |
Diseases |
Vitamin D-dependent Rickets, Type IA, Variant 2 |
Rachitismo dipendente dalla vitamina D, tipo IA, variante 2 |
Diseases |
Multiple Drug Resistance |
Resistenza multipla ai farmaci |
Diseases |
Autoimmune Lymphoproliferative Syndrome |
Sindrome linfoproliferativa autoimmune |
Diseases |
Congenital Myasthenic Syndrome |
Sindrome miastenica congenita |
Trait |
ABC Blood Group System |
Sistema del gruppo sanguigno ABC |
Trait |
Coat Type – Curly (Devon Rex, Selkirk Rex Type) or Hairless (Sphynx Type) – R Locus |
Tipo di pelo: riccio (tipo Devon Rex, Selkirk Rex) o glabro (tipo Sphynx) – locus R |