Browse CTGT's catalogue of NGS disorders and panels by disorder name.

C

Caffey disease COL1A1
Del Dup
NGS
Campomelic dysplasia SOX9
Del Dup
NGS
Camptodactyly, tall stature, and hearing loss syndrome FGFR3
Del Dup
NGS
Camurati-Engelmann disease TGFB1
Del Dup
NGS
Cantu syndrome ABCC9
Del Dup
NGS
Cantu syndrome NGS panel (2 genes) ABCC9, KCNJ8
Del Dup
NGS
Cantu syndrome, KCNJ8 related KCNJ8
Del Dup
NGS
Capillary malformation arteriovenous malformation RASA1
NGS
Del Dup
Cardiac channelopathy NGS panel (41 genes) ABCC9, AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, FGF12, GPD1L, HCN4, KCND2, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, NOS1AP, PKP2, RANGRF, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SEMA3A, SLMAP, SNTA1, TECRL, TRDN, TRPM4
Del Dup
NGS

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