List of AnyPanel disorder

PANEL TESTING GUIDE

Legend

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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Disease nameCategory

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