Genetic Test Details
Pediatric Cardiomyopathy panel
Test Information
- Titre
-
Pediatric Cardiomyopathy panel
- Catégorie
- Cardiogenetics
- Sub Category
-
Cardiomyopathy
- Gene/Platform/Region List
-
ABCC9, ACADVL, ACTC1, ACTN2, AGL, ALMS1, ALPK3, BAG3, BRAF, CACNA1C, CAV3, CBL, CPT2, CSRP3, CTNNA3, DES, DMD, DSC2, DSG2, DSP, DYSF, EMD, FHL1, FHOD3, FKRP, FKTN, FLNC, GAA, GATA4, GLA, HADHA, HADHB, HCN4, HRAS, JPH2, JUP, KLHL24, KRAS, LAMP2, LDB3, LMNA, LZTR1, MAP2K1, MAP2K2, MAP3K8, MIB1, MRAS, MTO1, MT-TI, MYBPC3, MYH7, MYL2, MYL3, MYO6, NEXN, NF1, NKX2-5, NRAP, NRAS, OBSCN, PKP2, PLEKHM2, PLN, PPA2, PPP1CB, PRDM16, PRKAG2, PTPN11, RAF1, RBM20, RIT1, RRAGD, RRAS, RRAS2, RYR2, SCN5A, SGCD, SHOC2, SLC22A5, SLC25A20, SLC25A4, SOS1, SOS2, SPRED2, TAB2, TAFAZZIN, TBX20, TBX5, TCAP, TMEM43, TMEM70, TNNC1, TNNI3, TNNI3K, TNNT2, TPM1, TRIM63, TTN, TTR, VCL
- Test type
- Gene Panel
- Samples Accepted
- Blood , DNA , Cultured Cells , Amniocyte , CVS
- Indications
- Diagnostics , Carrier Cascade Testing , Prenatal
- Test Methodology
- CNV , Sequencing
- Methodology Notes
-
Oligonucleotide based target capture, sanger sequencing for any clinically significant regions that are not captured and/or have insufficient coverage.
- Disease/Condition
-
Cardiomyopathy
Dernière Mise à Jour: 18 juin 2025