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DNA Laboratories Sdn Bhd
DNA Laboratories Sdn Bhd 200601017011 (736763-T)
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Products Clinical Genomics Testing Product 1 / 2

14-Oct-2022

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Categories: Clinical Genomics Testing
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PANEL TESTING GUIDE

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MIN MiniPanel™
MAX MaxPanel™
COM ComprehensivePanel™
+ PanelPlus®


For genes that require ancillary assays beyond NGS, we offer our PanelPlus® tests. All tests can expand to Whole Exome Sequencing, with new samples needed only for MiniPanel™ and MaxPanel™ testing tiers.

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Legend Disease Name Gene Category TestCode  
MAX Arrhythmia Panel, Comprehensive 73 genes Cardiology D4105
MAX Arrhythmia Panel, STAT Comprehensive 73 genes Cardiology D4105F
MAX Arrhythmogenic Cardiomyopathy Panel 24 genes Cardiology D4100
MAX Arrhythmogenic Cardiomyopathy Panel, STAT 24 genes Cardiology D4100F
MIN Brugada Syndrome Panel 8 genes Cardiology D4108
MIN Brugada Syndrome Panel, STAT 8 genes Cardiology D4108F
COM Cardiomyopathy Panel, Comprehensive 122 genes Cardiology D4101
COM Cardiomyopathy Panel, STAT Comprehensive 122 genes Cardiology D4101F
COM Cardiomyopathy and Skeletal Muscle Disease Panel 158 genes Cardiology D4109
COM Cardiomyopathy and Skeletal Muscle Disease Panel, STAT 158 genes Cardiology D4109F
MIN Catecholaminergic Polymorphic Ventricular Tachycardia Panel 10 genes Cardiology D5201
MAX Dilated Cardiomyopathy Panel 48 genes Cardiology D4102
MAX Dilated Cardiomyopathy Panel, STAT 48 genes Cardiology D4102F
MAX Hypertrophic Cardiomyopathy Panel 39 genes Cardiology D4103
MAX Hypertrophic Cardiomyopathy Panel, STAT 39 genes Cardiology D4103F
MAX Long QT Syndrome Panel 17 genes Cardiology D4106
MAX Long QT Syndrome Panel, STAT 17 genes Cardiology D4106F
MAX Marfan/TAAD Panel 25 genes Cardiology D4110
MAX Marfan/TAAD Panel, STAT 25 genes Cardiology D4110F
MIN Pulmonary Arterial Hypertension Panel 8 genes Cardiology D5226
MAX Deafness Non-Syndromic Sensorineural Autosomal Recessive Panel 46 genes Hearing loss D4401
MAX Deafness Non-Syndromic Sensorineural Autosomal Recessive Panel, STAT 46 genes Hearing loss D4401F
COM Hearing Loss Panel, Comprehensive 146 genes Hearing loss D5205
MAX Non-Syndromic Sensorineural Deafness Panel 60 genes Hearing loss D5223
MIN Treacher Collins Syndrome Sequencing Panel 3 genes Hearing loss D4405
MIN Treacher Collins Syndrome Sequencing Panel, STAT 3 genes Hearing loss D4405F
MIN Usher Syndrome Panel 14 genes Hearing loss D4308
MIN Usher Syndrome Panel, STAT 14 genes Hearing loss D4308F
MIN Waardenburg Syndrome Panel 7 genes Hearing loss D4402
MIN Waardenburg Syndrome Panel, STAT 7 genes Hearing loss D4402F
MAX Breast and Gynecological Cancers Panel 26 genes Hereditary Cancer D4210
MAX Breast and Gynecological Cancers Panel, STAT 26 genes Hereditary Cancer D4210F
MAX Cancer Panel, Comprehensive 82 genes Hereditary Cancer D4205
MAX Cancer Panel, STAT Comprehensive 82 genes Hereditary Cancer D4205F
MAX Colorectal Cancer Panel 19 genes Hereditary Cancer D4200
MAX Colorectal Cancer Panel 19 genes Hereditary Cancer D4200F
MIN Hereditary Breast and Ovarian Cancer Syndrome Panel 2 genes Hereditary Cancer D4209
MIN Hereditary Breast and Ovarian Cancer Syndrome Panel, STAT 2 genes Hereditary Cancer D4209F
MIN Lynch Syndrome Panel 5 genes Hereditary Cancer D5219
MIN Multiple Endocrine Neoplasias/Paraganglioma/Pheochromocytoma Panel 10 genes Hereditary Cancer D4203
MIN Multiple Endocrine Neoplasias/Paraganglioma/Pheochromocytoma Panel, STAT 10 genes Hereditary Cancer D4203F
MAX Pancreatic Cancer Panel 20 genes Hereditary Cancer D4201
MAX Pancreatic Cancer Panel, STAT 20 genes Hereditary Cancer D4201F
MAX Pediatric Tumor Panel 23 genes Hereditary Cancer D4207
MAX Pediatric Tumor Panel, STAT 23 genes Hereditary Cancer D4207F
MAX Renal Cancer Panel 25 genes Hereditary Cancer D4204
MAX Renal Cancer Panel, STAT 25 genes Hereditary Cancer D4204F
MIN Tuberous Sclerosis Panel 2 genes Hereditary Cancer D4211
MIN Tuberous Sclerosis Panel, STAT 2 genes Hereditary Cancer D4211F
+ Adrenoleukodystrophy Panel with ABCD1 15 genes Metabolic and Mitochondrial D4043
MIN Chronic Pancreatitis Panel 6 genes Metabolic and Mitochondrial D5202
+ Congenital Adrenal Hyperplasia Panel with CYP21A2 7 genes Metabolic and Mitochondrial D4584
+ Congenital Adrenal Hyperplasia Panel with CYP21A2, STAT 7 genes Metabolic and Mitochondrial D4584F
MAX Congenital Disorders of Glycosylation Panel 93 genes Metabolic and Mitochondrial D4571
MAX Congenital Disorders of Glycosylation Panel, STAT 93 genes Metabolic and Mitochondrial D4571F
MIN Congenital Hypothyroidism 8 genes Metabolic and Mitochondrial D4574
MIN Congenital Hypothyroidism, STAT 8 genes Metabolic and Mitochondrial D4574F
+ Creatine Deficiency Syndrome Panel 3 genes Metabolic and Mitochondrial D5209
MIN Elevated C4 Panel 3 genes Metabolic and Mitochondrial D4537
MIN Elevated C4 Panel, STAT 3 genes Metabolic and Mitochondrial D4537F
MIN Elevated C5-OH Panel 11 genes Metabolic and Mitochondrial D4541
MIN Elevated C5-OH Panel, STAT 11 genes Metabolic and Mitochondrial D4541F
MIN Elevated Phenylalanine Panel 5 genes Metabolic and Mitochondrial D4549
MIN Elevated Phenylalanine Panel, STAT 5 genes Metabolic and Mitochondrial D4549F
MAX Fatty Acid Oxidation Defects Panel 16 genes Metabolic and Mitochondrial D4572
MAX Fatty Acid Oxidation Defects Panel, STAT 16 genes Metabolic and Mitochondrial D4572F
MIN Galactosemia Panel 3 genes Metabolic and Mitochondrial D4563
MIN Galactosemia Panel, STAT 3 genes Metabolic and Mitochondrial D4563F
MAX Glycogen Storage Disease Panel, Comprehensive 23 genes Metabolic and Mitochondrial D4566
MAX Glycogen Storage Disease Panel, STAT Comprehensive 23 genes Metabolic and Mitochondrial D4566F
MAX Hyperammonemia Panel 48 genes Metabolic and Mitochondrial D5215
MIN Hyperparathyroidism Panel 8 genes Metabolic and Mitochondrial D5216
MIN Hereditary Hemochromatosis Panel 5 genes Metabolic and Mitochondrial D4700
MIN Hereditary Hemochromatosis Panel, STAT 5 genes Metabolic and Mitochondrial D4700F
MIN Krabbe Disease Panel 2 genes Metabolic and Mitochondrial D4506
MIN Krabbe Disease Panel, STAT 2 genes Metabolic and Mitochondrial D4506F
+ Lysosomal Storage Disorder Panel with GBA and IDS 12 genes Metabolic and Mitochondrial D3001
+ Lysosomal Storage Disorders Panel with GBA and IDS, Comprehensive 51 genes Metabolic and Mitochondrial D4501
+ Lysosomal Storage Disorders Panel with GBA and IDS, STAT Comprehensive 51 genes Metabolic and Mitochondrial D4501F
MIN Maple Syrup Urine Disease Panel 5 genes Metabolic and Mitochondrial D4561
MIN Maple Syrup Urine Disease Panel, STAT 5 genes Metabolic and Mitochondrial D4561F
MIN Metachromatic Leukodystrophy Panel 7 genes Metabolic and Mitochondrial D4508
MIN Metachromatic Leukodystrophy Panel, STAT 7 genes Metabolic and Mitochondrial D4508F
MAX Methylmalonic Acidemia Panel 17 genes Metabolic and Mitochondrial D4589
MAX Methylmalonic Acidemia Panel, STAT 17 genes Metabolic and Mitochondrial D4589F
COM Mitochondrial Encephalopathy/Leigh Syndrome Nuclear Gene Panel 146 genes Metabolic and Mitochondrial D4607
COM Mitochondrial Encephalopathy/Leigh Syndrome Nuclear Gene Panel, STAT 146 genes Metabolic and Mitochondrial D4607F
COM Mitochondrial Nuclear Gene Panel, Comprehensive 254 genes Metabolic and Mitochondrial D4606
COM Mitochondrial Nuclear Gene Panel, STAT Comprehensive 254 genes Metabolic and Mitochondrial D4606F
+ Mucopolysaccharidoses (MPS) Panel, Comprehensive 23 genes Metabolic and Mitochondrial D4502
+ Mucopolysaccharidoses (MPS) Panel, STAT Comprehensive 23 genes Metabolic and Mitochondrial D4502F
MAX Nephrotic Syndrome Panel 30 genes Metabolic and Mitochondrial D4613
MAX Nephrotic Syndrome Panel, STAT 30 genes Metabolic and Mitochondrial D4613F
MIN Primary Hyperoxaluria Panel 3 genes Metabolic and Mitochondrial D5225
MIN Tyrosinemia Panel 3 genes Metabolic and Mitochondrial D4562
MIN Tyrosinemia Panel, STAT 3 genes Metabolic and Mitochondrial D4562F
MIN Urea Cycle Disorders Panel 15 genes Metabolic and Mitochondrial D4532
MIN Urea Cycle Disorders Panel, STAT 15 genes Metabolic and Mitochondrial D4532F
+ Adrenoleukodystrophy Panel with ABCD1 15 genes Neurology D4043
MIN Aicardi-Goutieres Syndrome Panel 7 genes Neurology D4014
MIN Aicardi-Goutieres Syndrome Panel, STAT 7 genes Neurology D4014F
MIN Brain Iron Accumulation Syndromes Panel 9 genes Neurology D4016
MIN Brain Iron Accumulation Syndromes Panel, STAT 9 genes Neurology D4016F
MAX Brain Malformations Panel, Comprehensive 93 genes Neurology D4023
MAX Brain Malformations Panel, STAT Comprehensive 93 genes Neurology D4023F
MIN Ceroid Lipofuscinosis Panel 13 genes Neurology D4026
MIN Ceroid Lipofuscinosis Panel, STAT 13 genes Neurology D4026F
MAX Charcot Marie Tooth Disease Panel 62 genes Neurology D4037
MAX Charcot Marie Tooth Disease Panel, STAT 62 genes Neurology D4037F
MAX Dystonia Panel 17 genes Neurology D4012
MAX Dystonia Panel, STAT 17 genes Neurology D4012F
COM Epilepsy Panel, Comprehensive 99 genes Neurology D4002
COM Epilepsy Panel, STAT Comprehensive 99 genes Neurology D4002F
+ Expanded Leukodystrophy Panel with ABCD1 291 genes Neurology D5211
COM Focused Autism and Intellectual Disability Panel 263 genes Neurology D5130
COM Focused Autism and Intellectual Disability Panel, STAT 263 genes Neurology D5130F
MIN Hemiplegic Migraine Panel 4 genes Neurology D5213
MAX Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel 33 genes Neurology D4019
MAX Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel, STAT 33 genes Neurology D4019F
COM Hereditary Neuropathy Sequencing Panel 122 genes Neurology D4022
COM Hereditary Neuropathy Sequencing Panel, STAT 122 genes Neurology D4022F
MAX Infantile Epilepsy Panel 76 genes Neurology D4003
MAX Infantile Epilepsy Panel, STAT 76 genes Neurology D4003F
MAX Joubert and Meckel-Gruber Syndromes Panel 30 genes Neurology D4013
MAX Joubert and Meckel-Gruber Syndromes Panel, STAT 30 genes Neurology D4013F
MAX Lissencephaly Panel 24 genes Neurology D4025
MAX Lissencephaly Panel, STAT 24 genes Neurology D4025F
MIN Myoclonic Dystonia Panel 2 genes Neurology D4010
MIN Myoclonic Dystonia Panel, STAT 2 genes Neurology D4010F
MAX Nervous System and Brain Tumor Panel 17 genes Neurology D5222
MAX Neurodegeneration Panel 38 genes Neurology D4021
MAX Neurodegeneration Panel, STAT 38 genes Neurology D4021F
MAX Rett, Angelman and Related Syndromes Panel 20 genes Neurology D5203
MAX Spastic Paraplegia Panel Complete 55 genes Neurology D4011
MAX Spastic Paraplegia Panel Complete, STAT 55 genes Neurology D4011F
MAX Charcot Marie Tooth Disease Panel 62 genes Neuromuscular D4037
MAX Charcot Marie Tooth Disease Panel, STAT 62 genes Neuromuscular D4037F
MAX Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel 33 genes Neuromuscular D4019
MAX Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel, STAT 33 genes Neuromuscular D4019F
COM Hereditary Neuropathy Sequencing Panel 122 genes Neuromuscular D4022
COM Hereditary Neuropathy Sequencing Panel, STAT 122 genes Neuromuscular D4022F
MAX Hereditary Parkinson’s Disease and Parkinsonism Panel 21 genes Neuromuscular D4018
MAX Hereditary Parkinson’s Disease and Parkinsonism Panel, STAT 21 genes Neuromuscular D4018F
MAX Muscular Dystrophy Panel, Comprehensive 56 genes Neuromuscular D4032
MAX Muscular Dystrophy Panel, STAT Comprehensive 56 genes Neuromuscular D4032F
COM Neuromuscular Disorders Panel, Comprehensive 133 genes Neuromuscular D4035
COM Neuromuscular Disorders Panel, STAT Comprehensive 133 genes Neuromuscular D4035F
MAX Neuropathies Panel, Comprehensive 81 genes Neuromuscular D4020
MAX Neuropathies Panel, STAT Comprehensive 81 genes Neuromuscular D4020F
MAX Limb-Girdle Muscular Dystrophy Panel 30 genes Neuromuscular D5218
MIN Periodic Paralysis Panel 8 genes Neuromuscular D5224
MAX Albinism Panel 28 genes Ophthalmology D4309
MAX Albinism Panel, STAT 28 genes Ophthalmology D4309F
MAX Cataract Panel 69 genes Ophthalmology D5200
MIN Congenital Stationary Night-Blindness Panel 12 genes Ophthalmology D5207
COM Eye Disorders Panel, Comprehensive 211 genes Ophthalmology D4306
COM Eye Disorders Panel, Comprehensive STAT 211 genes Ophthalmology D4306F
MAX Glaucoma Panel 38 genes Ophthalmology D5212
MAX Leber Congenital Amaurosis Panel 19 genes Ophthalmology D5217
MIN Macular Dystrophy/Degeneration/Stargardt Disease Panel 15 genes Ophthalmology D4305
MIN Macular Dystrophy/Degeneration/Stargardt Disease Panel, STAT 15 genes Ophthalmology D4305F
MAX Microphthalmia/Anophthalmia/Coloboma Spectrum Panel 49 genes Ophthalmology D4300
MAX Microphthalmia/Anophthalmia/Coloboma Spectrum Panel, STAT 49 genes Ophthalmology D4300F
MIN Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Panel 15 genes Ophthalmology D4702
MIN Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Panel, STAT 15 genes Ophthalmology D4702F
COM Retina/Photoreceptor Dystrophy Panel 121 genes Ophthalmology D4304
COM Retina/Photoreceptor Dystrophy Panel, STAT 121 genes Ophthalmology D4304F
MAX Retinitis Pigmentosa Panel 66 genes Ophthalmology D4303
MAX Retinitis Pigmentosa Panel, STAT 66 genes Ophthalmology D4303F
MIN Usher Syndrome Panel 14 genes Ophthalmology D4308
MIN Usher Syndrome Panel, STAT 14 genes Ophthalmology D4308F
MIN Vitreoretinopathy Panel 4 genes Ophthalmology D5228
COM Ciliopathies Panel 101 genes Other Conditions D4703
COM Ciliopathies Panel, STAT 101 genes Other Conditions D4703F
MIN Cornelia de Lange Syndrome Panel 8 genes Other Conditions D4707
MIN Cornelia de Lange Syndrome Panel, STAT 8 genes Other Conditions D4707F
MIN Ehlers Danlos Panel 3 genes Other Conditions D5210
MIN Familial Mediterranean Fever Panel 9 genes Other Conditions D4730
MIN Familial Mediterranean Fever Panel, STAT 9 genes Other Conditions D4730F
MIN Hereditary Hemochromatosis Panel 5 genes Other Conditions D4700
MIN Hereditary Hemochromatosis Panel, STAT 5 genes Other Conditions D4700F
MIN Hereditary Hemorrhagic Telangiectasia Panel 5 genes Other Conditions D4734
MIN Hereditary Hemorrhagic Telangiectasia Panel, STAT 5 genes Other Conditions D4734F
MIN Hereditary Thrombophilia Panel 7 genes Other Conditions D4701
MIN Hereditary Thrombophilia Panel, STAT 7 genes Other Conditions D4701F
MIN Heterotaxy Panel 11 genes Other Conditions D4705
MIN Heterotaxy Panel, STAT 11 genes Other Conditions D4705F
MIN Holoprosencephaly Panel 10 genes Other Conditions D5214
MIN Hyper-IgE Syndromes Panel 4 genes Other Conditions D4712
MIN Hyper-IgE Syndromes Panel, STAT 4 genes Other Conditions D4712F
MAX Joubert and Meckel-Gruber Syndromes Panel 30 genes Other Conditions D4013
MAX Joubert and Meckel-Gruber Syndromes Panel, STAT 30 genes Other Conditions D4013F
MAX Limb Malformation: Sequencing Panel 40 genes Other Conditions D4725
MAX Limb Malformation: Sequencing Panel, STAT 40 genes Other Conditions D4725F
MAX MODY Panel 17 genes Other Conditions D4733
MAX MODY Panel, STAT 17 genes Other Conditions D4733F
MIN Myelodysplastic Syndrome/Leukemia Panel 14 genes Other Conditions D5220
MAX Noonan and RASopathies Panel 17 genes Other Conditions D4708
MAX Noonan and RASopathies Panel, STAT 17 genes Other Conditions D4708F
MAX Obesity Panel 35 genes Other Conditions D4731
MAX Obesity Panel, STAT 35 genes Other Conditions D4731F
MIN Periodic Fever Syndromes Panel 12 genes Other Conditions D4729
MIN Periodic Fever Syndromes Panel, STAT 12 genes Other Conditions D4729F
+ Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis 21 genes Other Conditions D4718
+ Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis, STAT 21 genes Other Conditions D4718F
MAX Pulmonary Disease: Comprehensive Sequencing Panel 52 genes Other Conditions D4732
MAX Pulmonary Disease: Comprehensive Sequencing Panel, STAT 52 genes Other Conditions D4732F
MIN Senior-Loken Syndrome Panel 9 genes Other Conditions D5227
MAX Skeletal Dysplasia with Increased Bone Density: Sequencing Panel 22 genes Other Conditions D4724
MAX Skeletal Dysplasia with Increased Bone Density: Sequencing Panel, STAT 22 genes Other Conditions D4724F
MIN Treacher Collins Syndrome Sequencing Panel 3 genes Other Conditions D4405
MIN Treacher Collins Syndrome Sequencing Panel, STAT 3 genes Other Conditions D4405F
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DNA Laboratories Sdn Bhd 200601017011 (736763-T)
B1-3 & B1-4, Block Plasma, UKM-MTDC Technology Centre, Universiti Kebangsaan Malaysia, 43650 Bangi, Selangor, Malaysia.

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