|
Clinical DNA Testing
Test
Requisition
Price
List
New Test Development
CAP / CLIA Certificates
|
|
CLICK ON THE LINKS
IN THE FOLLOWING LISTS FOR TEST DESCRIPTIONS AND TEST PRICES.
CPT Codes for each test are listed
at the bottom of the Test Descriptions.
PreventionGenetics offers a steadily
expanding menu of Clinical DNA tests. Our laboratory is CAP/CLIA
certified. Please use the Requisition
Form when ordering tests.
Tests Currently
Offered By Disease
Autosomal Recessive Polycystic Kidney Disease (PKHD1) |
Bernard-Soulier Syndrome (GP1BA, GP1BB, GP9)) |
Cardio-Facio-Cutaneous
Syndrome (BRAF, KRAS, MAP2K1, MAP2K2) |
| Cavernous Malformations
(KRIT1/CCM1, CCM2, PDCD10/CCM3) |
| Central Core Disease (RYR1) |
| CHARGE Syndrome (CHD7) |
| Congenital Disorders of Glycosylation (ALG6, MPI, PMM2) |
| Congenital Muscular Dystrophy (FCMD, FKRP, LAMA2, LARGE) |
| Costello Syndrome
(HRAS) |
| Cystic Fibrosis
(CFTR) |
| Dysferlin (DYSF)
|
| Dystonia (PNKD, GCH1, SGCE, TOR1A)
|
| Dystroglycanopathies |
| Fanconi-Bickel
Syndrome (SLC2A2) |
| Fingerprint
Panel |
| Fatty Acid Oxidation Disorders (ACADM, ACADS, ACADVL) |
| Fukuyama
Congenital Muscular Dystrophy
(FCMD) |
| Galactosemia (GALT) |
| Genome Polymorphism
Scan |
| Gender Panel |
GenMax™
|
Glutaric Acidemia
|
Glycogen
Storage Diseases (GYS2, G6PC, SLC37A4, GAA, AGL, GBE1, PYGM, PYGL, PFKM, PHKA2, PHKA1, PHKG2 SLC2A2) |
| Greig
Cephalopolysyndactyly Syndrome (GLI3) |
| HMG-CoA Lyase Deficiency (HMGCL) |
| Isovaleric Acidemia (IVD) |
| Joubert Syndrome
(AHI1, CEP290, TMEM67/MKS3, NPHP1) |
| Laminopathies
(LMNA) |
| LEOPARD Syndrome |
| Limb Girdle Muscular Dystrophy (CAPN3, DYSF, FCMD, FKRP, LMNA, POMT1, SGCA, SGCB) |
| Lymphedema
(FOXC2, FLT4) |
| Malignant
Hyperthermia (RYR1) |
| Mandibuloacral Dysplasia (LMNA, ZMPSTE24) |
| Meckel-Gruber Syndrome (MKS1, TMEM67/MKS3) |
| 3-Methylcrotonyl-CoA Carboxylase Deficiency (MCCC1, MCCC2) |
| Methylmalonic Acidemia(MMAA, MMAB, MUT) |
Multiminicore Disease (SEPN1) |
Multiple Carboxylase Deficiency (BTD, HLCS) |
| Muscle-Eye-Brain Disease (POMGNT1, POMT2) |
| N-acetylglucosaminyltransferase-like Protein(LARGE) |
| NeoNatal Testing(ACADM, ACADS, ACADVL, CFTR, GALT, HMGCL, IVD, MCCC1, MCCC2, MUT, PAH, PCCA, PCCB) |
| Nephronophthisis (NPHP1) |
| Noonan Syndrome
(PTPN11, RAF1, SOS1, KRAS) |
| Organic Acidemias
(HMGCL, IVD, MCCC1, MCCC2, MUT, PCCA, PCCB) |
| Pallister-Hall Syndrome (GLI3) |
| Phenylketonuria/Phenylalanine Hydroxylase Deficiency (PAH) |
| Progeria, Hutchinson-Gilford (LMNA) |
| Propionic Acidemia (PCCA, PCCB) |
| Protein O-mannose beta-1,2-N-acetylglucosaminyltransferase(POMGNT1) |
| Protein O-Mannosyltransferase 1 (POMT1) |
| Protein O-Mannosyltransferase 2 (POMT2) |
| Restrictive Dermopathy
(LMNA, ZMPSTE24) |
| Sarcoglycanopathies |
| SEPN1-Related Myopathies, Rigid Spine Muscular Dystrophy-1, Multiminicore Disease (SEPN1) |
| Smith-Lemli-Opitz Syndrome
(DHCR7) |
| Spondylocostal Dysostosis (DLL3, LFNG, MESP2) |
| Thrombocytopenia
(GATA1, GP1BA, GP1BB, GP9, MASTL, MPL, MYH9, RUNX1, WAS) |
| Thrombophilia
Panel (Factor V, Factor II, MTHFR) |
| Tyrosinemia (FAH) |
| Urea Cycle Disorders (OTC) |
| Ventricular
Tachycardia (RYR2) |
| Walker-Warburg Syndrome (FCMD, FKRP, LARGE, POMGNT1, POMT1, POMT2) |
| |
Tests
Currently Offered By Gene
Click on the links in the following list for test descriptions, test
prices and CPT codes.
- A -
- B -
- C -
- D -
Back to Top
- F -
- F2 Factor II (Prothrombin) G20210A Mutation Detection,Thrombophilia Panel
- F5 Factor V (Leiden) G1691A Mutation Detection, Thrombophilia Panel
- FAH Tyrosinemia, Type I
- FKRP Limb Girdle Muscular Dystrophy, Type 21; Congenital Muscular Dystrophy, Type 1C
- FKTN Fukuyama Congenital Muscular Dystrophy, Walker-Warburg Syndrome, Limb Girdle Muscular Dystrophy, Japanese Founder Mutation PCR
- FLT4 Hereditary Lymphedema, Type I (Milroy Disease)
- FOXC2 Lymphedema/Distichiasis Syndrome, Hereditary Lymphedema, Type II
- G -
- H -
Back to Top
- I -
- K -
- L -
- LAMA2 Congenital Muscular Dystrophy, Type 1A (Merosin-Deficient Congenital Muscular Dystrophy)
- LARGE N-acetylglucosaminyltransferase-like Protein
- LFNG Spondylocostal Dysostosis
- LMNA Atypical Werner Syndrome, Charcot-Marie-Tooth Neuropathy Type 2B1, Dilated Cardiomyopathy, Emery-Dreifuss Muscular Dystrophy, Familial Partial Lipodystrophy, Hutchinson-Gilford Progeria Syndrome, Lethal Tight Skin Contracture Syndrome (Restrictive Dermopathy), Limb-Girdle Muscular Dystrophy Type 1B, Lipoatrophy, LMNA-Related Dilated Cardiomyopathy, Mandibuloacral Dysplasia
Back to Top
- M -
- N -
- O -
- P -
Back to Top
- R -
- S -
- T -
- W -
- Z -
Back to Top
|
