Combination Pack CombiGen Dog

Below you find all tests present in the CombiGen Dog and CombiGen Dog Plus Combination package.  For specific information about these DNA test we refer you to our local distributors.

CombiGen Dog (H669)

CombiGen Dog Plus (H670)

H301 PAP-PRA1 2
H303 Spinocerebellar ataxia
H304 Ichthyosis 3
H305 PAP-PRA1 1
H306 Multifocal Retinopathy 3 (cmr3) 1
H307 Multifocal Retinopathy 3 (cmr3) 2
H308 Degenerative Myelopathy 2 (DM2 Bernese mountain)
H312 Craniomandibular Osteopathy (CMO)
H351 Amelogenesis Imperfecta
H355 Cerebellar Hypoplasia Resembling
H356 Chondrodysplasia, Disproportionate Short-Limbed
H357 Cone Rod Dystrophy 1 (crd1)
H358 Cone Rod Dystrophy 2 (crd2)
H360 Gallbladder Mucocele
H363 Hyperkeratosis, epidermolytic
H364 Hypocatalasia
H366 IGS (Selective Cobalamin Malabsorption) 1
H367 IGS (Selective Cobalamin Malabsorption) 2
H368 Myopathy
H370 Nephritis
H371 PRA
H372 PRA crdPRA
H373 PRA type 3
H374 Primary Hyperoxaluria
H375 Dog_Skin Fragility
H382 PRA erd
H383 Primary Glaucoma
H414 Primary Ciliary dyskinesia
H421 Hiplaxity 2
H424 Musladin-Lueke syndrome (MLS)
H427 MTM
H435 Factor VII deficiency
H450 Bleeding disorder due to P2RY12 defect
H456 SCID 2
H473 GR_PRA2
H487 Brachyury (Bobtail)
H493 Muscular hypertrophy (double muscling)
H510 Skeletal Dysplasia 2 (SD2)
H511 rcd4 PRA
H607 Factor IX Deficiency
H697 Narcolepsy 2
H698 Narcolepsy 3
H699 Hereditary Cataract 2 (HSF4)
H701 Coppertoxicosis
H703 Cystinuria I - A - 1
H709 CLAD, Type I
H717 PFK (Phosphofructokinase Deficiency)
H724 L2-HGA
H728 CSNB (Congenital Stationary Night Blindness)
H730 CMR2 (Canine Multifocal Retinopathy)
H733 Coat Colour B-locus
H734 Coat Colour E-locus
H738 Myotonia Congenita
H740 Pyruvate Dehydrogenase Phosphatase 1 (PDP1)
H741 Pyruvate kinase Deficiency (PKDef)
H748 Mucopolysaccharidosis Type VII
H749 Centronuclear Myopathy (CNM, also known as HMLR)
H765 Hair length
H766 crd4-PRA (previously cord1-PRA)
H768 rcd1 PRA
H770 rcd3 PRA
H787 Trapped Neutrophil Syndrome (TNS)
H804 Cerebellar Ataxia / NCL-A
H809 Hereditary Cataract (HC) - HSF4
H811 Hyperuricemia (HUU)
H812 Neonatal Encephalopathy
H818 Coat Colour Em-locus
H847 Coat Colour D-Locus Improved (MLPH)
H849 Primary Lens Luxation (PLL)
H868 GR_PRA1
H871 CMR1 (Canine Multifocal Retinopathy)
H872 Pituitary dwarfism
H873 Ichthyosis 2
H913 Dry Eye Curly Coat Syndrome
H919 Hiplaxity 1

H723 MDR1
H301 PAP-PRA1 2
H303 Spinocerebellar ataxia
H304 Ichthyosis 3
H305 PAP-PRA1 1
H306 Multifocal Retinopathy 3 (cmr3) 1
H307 Multifocal Retinopathy 3 (cmr3) 2
H308 Degenerative Myelopathy 2 (DM2 Bernese mountain)
H312 Craniomandibular Osteopathy (CMO)
H351 Amelogenesis Imperfecta
H355 Cerebellar Hypoplasia Resembling
H356 Chondrodysplasia, Disproportionate Short-Limbed
H357 Cone Rod Dystrophy 1 (crd1)
H358 Cone Rod Dystrophy 2 (crd2)
H360 Gallbladder Mucocele
H363 Hyperkeratosis, epidermolytic
H364 Hypocatalasia
H366 IGS (Selective Cobalamin Malabsorption) 1
H367 IGS (Selective Cobalamin Malabsorption) 2
H368 Myopathy
H370 Nephritis
H371 PRA
H372 PRA crdPRA
H373 PRA type 3
H374 Primary Hyperoxaluria
H375 Dog_Skin Fragility
H382 PRA erd
H383 Primary Glaucoma
H414 Primary Ciliary dyskinesia
H421 Hiplaxity 2
H424 Musladin-Lueke syndrome (MLS)
H427 MTM
H435 Factor VII deficiency
H450 Bleeding disorder due to P2RY12 defect
H456 SCID 2
H473 GR_PRA2
H487 Brachyury (Bobtail)
H493 Muscular hypertrophy (double muscling)
H510 Skeletal Dysplasia 2 (SD2)
H511 rcd4 PRA
H607 Factor IX Deficiency
H697 Narcolepsy 2
H698 Narcolepsy 3
H699 Hereditary Cataract 2 (HSF4)
H701 Coppertoxicosis
H703 Cystinuria I - A - 1
H709 CLAD, Type I
H717 PFK (Phosphofructokinase Deficiency)
H724 L2-HGA
H728 CSNB (Congenital Stationary Night Blindness)
H730 CMR2 (Canine Multifocal Retinopathy)
H733 Coat Colour B-locus
H734 Coat Colour E-locus
H738 Myotonia Congenita
H740 Pyruvate Dehydrogenase Phosphatase 1 (PDP1)
H741 Pyruvate kinase Deficiency (PKDef)
H748 Mucopolysaccharidosis Type VII
H749 Centronuclear Myopathy (CNM, also known as HMLR)
H765 Hair length
H766 crd4-PRA (previously cord1-PRA)
H768 rcd1 PRA
H770 rcd3 PRA
H787 Trapped Neutrophil Syndrome (TNS)
H804 Cerebellar Ataxia / NCL-A
H809 Hereditary Cataract (HC) - HSF4
H811 Hyperuricemia (HUU)
H812 Neonatal Encephalopathy
H818 Coat Colour Em-locus
H847 Coat Colour D-Locus Improved (MLPH)
H849 Primary Lens Luxation (PLL)
H868 GR_PRA1
H871 CMR1 (Canine Multifocal Retinopathy)
H872 Pituitary dwarfism
H873 Ichthyosis 2
H913 Dry Eye Curly Coat Syndrome
H919 Hiplaxity 1

Version: 2017-01-16

Please be aware that in rare cases not all markers will be reported. If you need a result for one specific marker imperatively, we advise you to order the single test for that particular marker. In this way you will make sure you will always get a result.