BROWN / BLACK ROSETTE - Daughter of Exotic Legends King Titan & Exotic Legends Astarte Grace (Rene)
She has been placed with Viper - we are hoping for a stunning litter
Pedigree includes RW SGC, CH, DCG, RW QGC and more. She is super soft and super friendly. She has oval, almost round large eyes. She is VERY vocal and talks all the time. SUPER SOFT. She has a full and broad muzzle, and prominent whisker pads. She has a FAT tail, but most importantly she is very seet, loving and gentle. A wonderful example of the breed.
The following are Sundari's Parents results from the testing we have conducted - You can also check out our Sire and Dam page for her parents and her grandparents results. Sundari is 100% clear:
HCM -CLEAR - TITAN 7-5-2019 HCM SCAN.pd
The following are Sundari 's results from the testing we have conducted:
Acute Intermittent Porphyria (Variant 1) - Negative
Acute Intermittent Porphyria (Variant 2) - Negative
Acute Intermittent Porphyria (Variant 3) - Negative
Acute Intermittent Porphyria (Variant 4) - Negative
Acute Intermittent Porphyria (Variant 5) - Negative
Autoimmune Lymphoproliferative Syndrome - Negative
Burmese Head Defect (Discovered in Burmese) - Negative
Chediak-Higashi Syndrome (Discovered in Persian cats) - Negative
Congenital Adrenal Hyperplasia - Negative
Congenital Erythropoietic Porphyria - Negative
Congenital Myasthenic Syndrome (Discovered in Devon Rex and Sphynx) - Negative
Cystinuria Type 1A - Negative
Cystinuria Type B (Variant 1) - Negative
Cystinuria Type B (Variant 2) - Negative
Cystinuria Type B (Variant 3) - Negative
Dihydropyrimidinase Deficiency - Negative
Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold) - Negative
Factor XII Deficiency (Variant 1) - Negative
Factor XII Deficiency (Variant 2) - Negative
Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese) - Negative
GM1 Gangliosidosis - Negative
GM2 Gangliosidosis - Negative
GM2 Gangliosidosis, type II (Discovered in Burmese cats) - Negative
GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats) - Negative
GM2 Gangliosidosis, type II (Discovered in japanese domestic cats) - Negative
Glutaric Aciduria Type II - Negative
Glycogen Storage Disease (Discovered in Norwegian Forest Cat) - Negative
Hemophilia B (Variant 1) - Negative
Hemophilia B (Variant 2) - Negative
Hyperoxaluria type II - Negative
Hypertrophic Cardiomyopathy (A31P; Discovered in Maine Coon) - Negative
Hypertrophic Cardiomyopathy (Discovered in Ragdoll) - Negative
Hypotrichosis (Discovered in Birman cats) - Negative
Lipoprotein Lipase Deficiency - Negative
Medication Sensitivity (MDR1) - Negative
Mucopolysaccharidosis Type I - Negative
Mucopolysaccharidosis Type VI (mild form) - Negative
Mucopolysaccharidosis Type VI (severe) - Negative
Mucopolysaccharidosis Type VII - Negative
Mucopolysaccharidosis VII - Negative
Myotonia Congenita - Negative
Polycystic Kidney Disease (PKD) - Negative
Progressive Retinal Atrophy (Discovered in Bengal cats) - Negative
Progressive Retinal Atrophy (Discovered in Persian cats) - Negative
Progressive Retinal Atrophy (rdAc-PRA) - Negative
Pyruvate Kinase Deficiency - Negative
Sphingomyelinosis (Variant 1) - Negative
Sphingomyelinosis (Variant 2) - Negative
Spinal Muscular Atrophy (Discovered in Maine Coon) - Negative
Vitamin D-Dependent Rickets - Negative
F.I.V. - Negative
FeLV - Negative
DNA Coat Color: -