Abaixo, pode encontrar todos os testes dos Pacotes Combinados CombiGen Cão e CombiGen Cão Plus. Para informações específicas sobre todos estes testes, contacte os nossos distribuidores locais especializados.
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CombiGen Dog (H669)
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CombiGen Dog Plus (H670)
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H348 PAP-PRA1
H303 Spinocerebellar ataxia
H304 Ichthyosis 3
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
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H629 MDR1 (partner lab)
H348 PAP-PRA1
H303 Spinocerebellar ataxia
H304 Ichthyosis 3
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
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Version: 2018-11-07
Tenha em atenção que, em casos raros, nem todos os marcadores serão reportados. Se precisar de um resultado para um marcador específico de forma imperativa, aconselhamo-lo a solicitar o teste único para esse marcador em particular. Desta forma, assegura que irá obter o resultado.