Imię i przydomek:Ruykirags VENICE
Rodowód: pokażData urodzenia:08.04.2024
Umaszczenie (EMS): lilac bicolour (RAG c 03)
Rodzice: Ojciec: SIRIUS GEMME PREZIOSE
pokaż rodowód ojcaMatka: DGC RUYKIRAGS PEILING
pokaż rodowód matkiZdrowie:Grupa krwi: A
Masa: 6000g
Badania genetyczne:Wszystkie wyniki negatywne N/N (CLEAR):
m.in.:
HCM – Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
HCM – Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
PKD – Polycystic Kidney Disease (PKD)
i wiele innych:
- Acute Intermittent Porphyria (Variant 2)
- Acute Intermittent Porphyria (Variant 3)
- Acute Intermittent Porphyria (Variant 4)
- Acute Intermittent Porphyria (Variant 5) – NEW!
- Autoimmune Lymphoproliferative Syndrome
- Blood Type
- Burmese Head Defect
- Chediak-Higashi Syndrome (Discovered in Persian cats) – NEW!
- Congenital Adrenal Hyperplasia
- Congenital Erythropoietic Porphyria
- Congenital Myasthenic Syndrome
- Cystinuria Type 1A
- Cystinuria Type B (Variant 1)
- Cystinuria Type B (Variant 2)
- Cystinuria Type B (Variant 3)
- Dihydropyrimidinase Deficiency
- Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold)
- Factor XII Deficiency (Variant 1)
- Factor XII Deficiency (Variant 2) – NEW!
- Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese)
- Glutaric Aciduria Type II – NEW!
- Glycogen Storage Disease
- GM1 Gangliosidosis
- GM2 Gangliosidosis
- GM2 Gangliosidosis, type II (Discovered in Burmese cats) – NEW!
- GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats)
- GM2 Gangliosidosis, type II (Discovered in japanese domestic cats)
- Hemophilia B (Variant 1)
- Hemophilia B (Variant 2)
- Hyperoxaluria type II
- Hypertrophic Cardiomyopathy (Discovered in Maine Coon)
- Hypertrophic Cardiomyopathy (Discovered in Ragdoll)
- Hypotrichosis (Discovered in Sacred Birman)
- Lipoprotein Lipase Deficiency
- Mucopolysaccharidosis Type I
- Mucopolysaccharidosis Type VI (G1558A variant) – NEW!
- Mucopolysaccharidosis Type VI (T1427C variant)
- Mucopolysaccharidosis Type VII
- Mucopolysaccharidosis VII
- Multidrug Resistance 1
- Myotonia Congenita
- Polycystic Kidney Disease (PKD)
- Progressive Retinal Atrophy (rdAc-PRA)
- Progressive Retinal Atrophy (Discovered in Bengal cats)
- Progressive Retinal Atrophy (Discovered in Persian cats) – NEW!
- Pyruvate Kinase Deficiency
- Sphingomyelinosis (Variant 1)
- Sphingomyelinosis (Variant 2)
- Spinal Muscular Atrophy
- Vitamin D-Dependent Rickets