ragdoll_katzen


Granya from Sherman Hill cream sepia mitted trägt chocolate geb. am 19.04.2020 Blutgruppe: A Mucopolysaccharidosis N/N Pyruvate Kinase Deficiency (PK) N/N Polycystic Kidney Disease (PKD1) N/N Niemann Pick Disease-Sphyingomyelinosis N/N Hypertrophic Cardiomyopathy (HCM 1+2) N/N Progressive Retinal Atrophy (PRA-RDC) N/N Spinal Muscular Atrophy (SMA) N/N Gylcogen Storage Disease Type IV N/N Gangliosodosis Type 1+2 N/N Hereditary Retinal Degeneration PRA N/N Burmese Hypokalamemia Periodic Polymyopathy N/N FelV + FiV negativ getestet
	Romy from Sherman Hill (Kastrat) black tortie solid mitted geb. am 23.06.2018 trägt Verdünnung Blutgruppe: A Mucopolysaccharidosis N/N Pyruvate Kinase Deficiency (PK) N/N Polycystic Kidney Disease (PKD1) N/N Niemann Pick Disease-Sphyingomyelinosis N/N Hypertrophic Cardiomyopathy (HCM 1+2) N/N Progressive Retinal Atrophy (PRA-RDC) N/N Spinal Muscular Atrophy (SMA) N/N Gylcogen Storage Disease Type IV N/N Gangliosodosis Type 1+2 N/N Hereditary Retinal Degeneration PRA N/N Burmese Hypokalamemia Periodic Polymyopathy N/N FelV + FiV negativ getestet
Aramis de Neria Regina blue lynx point mitted geb. am 29.08.2018 trägt chocolate Blutgruppe: A Mucopolysaccharidosis N/N Pyruvate Kinase Deficiency (PK) N/N Polycystic Kidney Disease (PKD1) N/N Niemann Pick Disease-Sphyingomyelinosis N/N Hypertrophic Cardiomyopathy (HCM 1+2) N/N Progressive Retinal Atrophy (PRA-RDC) N/N Spinal Muscular Atrophy (SMA) N/N Gylcogen Storage Disease Type IV N/N Gangliosodosis Type 1+2 N/N Hereditary Retinal Degeneration PRA N/N Burmese Hypokalamemia Periodic Polymyopathy N/N FelV + FiV negativ getestet
	Nuri from Sherman Hill seal tortie mink mitted geb. am 11.07.2021 Blutgruppe: A trägt Verdünnung und chocolate FelV + FiV negativ getestet Mucopolysaccharidosis N/N Pyruvate Kinase Deficiency (PK) N/N Polycystic Kidney Disease (PKD1) N/N Niemann Pick Disease-Sphyingomyelinosis N/N Hypertrophic Cardiomyopathy (HCM 1+2) N/N Progressive Retinal Atrophy (PRA-RDC) N/N Spinal Muscular Atrophy (SMA) N/N Gylcogen Storage Disease Type IV N/N Gangliosodosis Type 1+2 N/N Hereditary Retinal Degeneration PRA N/N Burmese Hypokalamemia Periodic Polymyopathy N/N FelV + FiV negativ getestet