Browse CTGT's catalogue of NGS disorders and panels by disorder name.
|Ichthyosis NGS panel (28 genes)||ABCA12, ALOX12B, ALOXE3, CASP14, CDSN, CERS3, CHST8, CSTA, CYP4F22, FLG, GJA1, GJB3, GJB4, KDSR, KRT1, KRT10, KRT2, LIPN, LOR, NIPAL4, PNPLA1, POMP, SERPINB8, ST14, STS, SULT2B1, TGM1, TGM5|
|Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1||VCP|
|Insulin-like growth factor I deficiency||IGF1|
|Insulin-like growth factor I deficiency and Insulin-like growth factor I, resistance to NGS panel (2 genes)||IGF1, IGF1R|
|Insulin-like growth factor I, resistance to||IGF1R|