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My CombiBreed
Info results
Results and inheritance
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Search test(s) for your breed
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
K866
CombiBreed Coat Colour
K865
CombiBreed Genetic Diseases
K460
CombiBreed Hair Length
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)
K764
Hypertrophic Cardio Myopathy 2 (HCM2)
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)
Other genetic traits
K793
Bloodtyping AB (DNA test)
K712
Bloodtyping AB (Serology)
K757
Coat Colour Agouti
K314
Coat Colour Albino
K759
Coat Colour Burmese
K756
Coat Colour Chocolate
K755
Coat Colour Cinnamon
K760
Coat Colour Dilution
K303
Coat colour Dominant White & White Spotting
K639
Coat Colour E locus, extension
K306
Coat colour Russet (Burmese)
K758
Coat Colour Siamese
K502
Cornish Rex, Curly/woolly coat
K304
Devon Rex, Curly Coat
K466
Hair Length all breeds
K461
Hair Length Maine Coon
K462
Hair Length Norwegian Forest
K463
Hair Length Ragdoll
K305
Sphynx, Hairless Coat
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Cat
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