When your veterinarian suspects a genetic cause for your cat’s otherwise unexplainable symptoms, MoxxiTech is here to help.
RALLEE® Certified Feline Diagnostic Panel 3 includes genetic testing for diseases with symptoms involving blood, endocrine system, gastrointestinal tract, heart, immune system, kidneys, liver, and reproduction that may be difficult to accurately diagnose clinically due to rarity or due to broad symptoms that are common to multiple diseases. Understanding the specific genetic cause for your cat’s symptoms allows your veterinarian to identify the best treatment possible, potentially including enrollment in experimental therapies.
Learn more about genetic testing Order a Sample Collection Kit Veterinarians: Order Now
Number of Alleles Tested: 40 |
|
Condition |
Gene(s) |
Acute Intermittent Porphyria (AIP) 1-6 |
HMBS |
Autoimmune Lymphoproliferative Syndrome (ALPS) |
FASL |
Chediak-Higashi Syndrome |
LYST |
Congenital Hypothyroidism |
TPO |
Cystinuria Type IA |
SLC3A1 |
Cystinuria Type IB 1-4 |
SLC7A9 |
Cystinuria Type IIB |
SLC7A9 |
Dihydropyrimidinase (DHP) |
CPYS |
Erythrocyte Pyruvate Kinase Deficiency (PK Deficiency) |
PKLR |
Erythropoietic Porphyria |
UROS |
Factor XII Deficiency 1, 2 |
F12 |
Glycogen Storage Disease Type IV (GSD IV) |
GBE |
Hemophilia B 1, 2 |
F9 |
Hepatic Copper Accumulation |
ATP7B |
Hyperlipoproteinaemia |
LPL |
Hyperoxaluria Type II |
GRHPR |
Hypertrophic Cardiomyopathy (HCM) 1-3 |
MYBPC3, MYH7 |
Leukocyte Adhesion Deficiency Type I |
ITGB2 |
Methemoglobinemia 1, 2 |
CYB5R3 |
Mucolipidosis II |
GNPTAB |
Mucopolysaccharidosis Type I |
IDUA |
Niemann-Pick Disease Type C1 (NPC1) 1, 2 |
NPC1 |
Niemann-Pick Disease Type C2 (NPC2) |
NPC2 |
Polycystic Kidney Disease (PKD) |
PKD1 |
Resistance to FIV 1 |
APOBEC3C |
Testicular Hypoplasia and Persistent Primary Dentition 1 |
TAC3 |