CatCheck List of Items Tested | ||
---|---|---|
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 |