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MyCatDNA™+ DNA Profile with Parentage Service (health test)

Included Health Tests

  • Acute Intermittent Porphyria (Variant 1)
  • 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