EXOTIC LEGENDS FLAMING SAPPHIRE


EXOTIC LEGENDS FLAMING SAPPHIRE

Sapphire is the daughter of CH Viper and Destiny. 

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 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 Sapphire's results from the testing we have conducted:

HCM - To young to test

Bengal PRA - N/N by percentage - Parents results on this site

Pyruvate Kinase Deficiency (PK) -  N/N by percentage - Parents results on this site

Acute Intermittent Porphyria (Variant 1) - Clear 

Acute Intermittent Porphyria (Variant 2) - Clear 

Acute Intermittent Porphyria (Variant 3) - Clear 

Acute Intermittent Porphyria (Variant 4) - Clear 

Acute Intermittent Porphyria (Variant 5) - Clear 

Autoimmune Lymphoproliferative Syndrome - Clear 

Burmese Head Defect (Discovered in Burmese) - Clear

Chediak-Higashi Syndrome (Discovered in Persian cats) - Clear 

Congenital Adrenal Hyperplasia - Clear 

Congenital Erythropoietic Porphyria - Clear 

Congenital Myasthenic Syndrome (Discovered in Devon Rex and Sphynx) - Clear 

Cystinuria Type 1A - Clear 

Cystinuria Type B (Variant 1) - Clear 

Cystinuria Type B (Variant 2) - Clear 

Cystinuria Type B (Variant 3) - Clear 

Dihydropyrimidinase Deficiency - Clear 

Earfold and Osteochondrodysplasia (Discovered in the Scottish Fold) - Clear 

Factor XII Deficiency (Variant 1) - Clear 

Factor XII Deficiency (Variant 2) - Clear

Familial Episodic Hypokalaemic Polymyopathy (Discovered in Burmese) - Clear 

GM1 Gangliosidosis - Clear 

GM2 Gangliosidosis - Clear 

GM2 Gangliosidosis, type II (Discovered in Burmese cats) - Clear

GM2 Gangliosidosis, type II (Discovered in domestic shorthair cats) - Clear 

GM2 Gangliosidosis, type II (Discovered in japanese domestic cats) - Clear 

Glutaric Aciduria Type II - Clear 

Glycogen Storage Disease (Discovered in Norwegian Forest Cat) - Clear

Hemophilia B (Variant 1) - Clear 

Hemophilia B (Variant 2) - Clear 

Hyperoxaluria type II - Clear 

Hypertrophic Cardiomyopathy (A31P; Discovered in Maine Coon) - Clear 

Hypertrophic Cardiomyopathy (Discovered in Ragdoll) - Clear 

Hypotrichosis (Discovered in Birman cats) - Clear 

Lipoprotein Lipase Deficiency - Clear 

Medication Sensitivity (MDR1) - Clear 

Mucopolysaccharidosis Type I - Clear 

Mucopolysaccharidosis Type VI (mild form) - Clear 

Mucopolysaccharidosis Type VI (severe) - Clear

Mucopolysaccharidosis Type VII - Clear 

Mucopolysaccharidosis VII - CLear 

Myotonia Congenita - Clear 

Polycystic Kidney Disease (PKD) - Clear 

Progressive Retinal Atrophy (Discovered in Bengal cats) - Clear 

Progressive Retinal Atrophy (Discovered in Persian cats) - Clear 

Progressive Retinal Atrophy (rdAc-PRA) - Clear

Pyruvate Kinase Deficiency - Clear 

Sphingomyelinosis (Variant 1) - Clear

Sphingomyelinosis (Variant 2) - Clear 

Spinal Muscular Atrophy (Discovered in Maine Coon) - Clear 

Vitamin D-Dependent Rickets - Clear 

F.I.V. - Negative 

FeLV - Negative 

DNA Coat Color -