Animals - Cat : Combibreed

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Breed

Include tests which are not breed specific

Cat

Kinship, Parentage and Identity

K205 DNA profile Cat

K202 Maternity Verification Cat

K200 Parentage Verification Cat

K201 Paternity Verification Cat

Combination Packages

K875 CombiBreed Bengal

K872 CombiBreed British Short hair and Long hair

K868 CombiBreed Burmese

K866 CombiBreed Coat Colour

K879 CombiBreed Devon Rex

K865 CombiBreed Genetic Diseases

K460 CombiBreed Hair Length

K869 CombiBreed Maine Coon

K876 CombiBreed Norwegian Forest Cat

K871 CombiBreed Persian

K870 CombiBreed Ragdoll

K874 CombiBreed Sacred Birman

K880 CombiBreed Savannah

K878 CombiBreed Siamese, Oriental short hair

K873 CombiBreed Siberian Cat

K877 CombiBreed Sphynx

Genetic diseases

K302 Alpha-Mannosidosis

K310 Autoimmune Lymphoproliferative Syndrome (ALPS)

K316 Bengal Prog. Retinal Atrophy (PRA-b) (service lab)

K608 Brachycephaly (Frontonasal Dysplasia (FND))

K597 Congenital Adrenal Hyperplasia

K598 Dihydropyrimidinase Deficiency

K315 Ehlers-Danlos syndrome, classic type

K385 Factor XII Deficiency

K312 Feline Leukocyte Adhesion Deficiency (CD18, FLAD)

K898 Gangliosidosis, GM1

K646 Gangliosidosis, GM2, GM2A

K640 Gangliosidosis, GM2, type II - 1

K647 Gangliosidosis, GM2, type II - 2

K309 Gangliosidosis, GM2, type II - 3

K751 Glycogentoxicosis GSD Type IV

K656 Haemophilia B - 1

K657 Haemophilia B - 2

K400 Hereditary Myopathy (CMS; Cong. Myas. Syndrome)

K599 Hyperlipoproteinaemia

K725 Hypertrophic Cardio Myopathy 1 (HCM1)

K799 Hypertrophic Cardio Myopathy 3 (HCM3)

K649 Hypothyroidism

K390 Hypotrichosis, with short life expectancy

K389 Hypotrichosis, with whiskers short and curled 1

K386 Mucopolysaccharidosis I

K651 Mucopolysaccharidosis VI

K650 Mucopolysaccharidosis VII

K384 Mucopolysaccharidosis VII (2)

K397 Mucopolysaccharidosis VII (3)

K600 Niemann-Pick C1 Disease

K311 Niemann-Pick Syndrome Type C1

K399 Osteochondrodysplasia (Fold Mutation)

K504 Periodic paralysis (WNK4 - Hypokalemia)

K711 Polycystic Kidney Disease (PKD)

K388 Porphyria, Acute Intermittent (4) 1

K392 Porphyria, Acute Intermittent (4) 2

K393 Porphyria, Acute Intermittent (4) 3

K394 Porphyria, Acute Intermittent (4) 4

K395 Porphyria, Acute Intermittent (4) 5

K396 Porphyria, Acute Intermittent (4) 6

K387 Porphyria, Congenital Erythropoietic (2) 1

K391 Porphyria, Congenital Erythropoietic (2) 2

K601 Primary Hyperoxaluria II

K762 Progressive Retinal Atrophy (rdAc-PRA)

K867 Progressive Retinal Atrophy (Rdy-PRA)

K754 Pyruvaatkinase Deficiency (PKDef)

K767 Spinal Muscular Atrophie (SMA)

K641 Vitamin D-deficiency rickets, type I

Test on demand

K300 Bloodtyping AB (DNA test Ragdoll Cats)

K317 MC1R cat rare allele

K313 PRA (early onset)