Browse CTGT's test catalogue, including NGS panels, by test code.

Test Codesort ascending Disorder or Panel Test Method
1136 Ehlers-Danlos syndrome, vascular type
Del Dup
1135 Ehlers-Danlos syndrome, vascular type
NGS
1134 Ehlers-Danlos syndrome, classic type NGS panel
NGS
1133 Ehlers-Danlos syndrome, classic type, 2
Del Dup
1132 Ehlers-Danlos syndrome, classic type, 2
NGS
1131 Ehlers-Danlos syndrome, classic type, I
Del Dup
1130 Ehlers-Danlos syndrome, classic type, I
NGS
1129 Ehlers-Danlos syndrome, spondylodysplastic type, 3
NGS
1128 Ehlers-Danlos syndrome, musculocontractural type, 1
Del Dup
1127 Ehlers-Danlos syndrome, musculocontractural type, 1
NGS
1126 Ectopia lentis, isolated, autosomal recessive
Del Dup
1125 Ectopia lentis, isolated, autosomal recessive
NGS
1124 Ectopia lentis, isolated, autosomal dominant
Del Dup
1123 Ectopia lentis, isolated, autosomal dominant
NGS
1122 Dyssegmental dysplasia, Silverman-Handmaker type
Del Dup
1121 Dyssegmental dysplasia, Silverman-Handmaker type
NGS
1120 Dyggve-Melchior-Clausen disease
Del Dup
1119 Dyggve-Melchior-Clausen disease
NGS
1118 Digital arthropathy-brachydactyly, familial
NGS
1117 Diastrophic dysplasia
Del Dup
1116 Diastrophic dysplasia
Sanger
1115 Diaphanospondylodysostosis
NGS
1114 Desbuquois dysplasia 1
Del Dup
1113 Desbuquois dysplasia 1
NGS
1112 Cutis laxa, autosomal recessive 1A
Del Dup
1111 Cutis laxa, autosomal recessive 1A
Sanger
1110 Cutis laxa, autosomal recessive 1B
Del Dup
1109 Cutis laxa, autosomal recessive 1B
NGS
1108 Cutis laxa, autosomal dominant 2 & autosomal recessive, type IA
Del Dup
1107 Cutis laxa, autosomal dominant 2 & autosomal recessive, type IA
NGS
1106 FGFR2 related craniosynostosis
Del Dup
1105 FGFR2 related craniosynostosis
NGS
1104 FGFR1, FGFR2, FGFR3 & TWIST1 related craniosynostosis panel
Sanger
1103 FGFR1, FGFR2 and FGFR3 related craniosynostosis panel
Sanger
1102 Saethre-Chotzen syndrome
Del Dup
1101 Saethre-Chotzen syndrome
Sanger
1099 Pfeiffer syndrome
Sanger
1098 Muenke syndrome
Sanger
1097 Jackson-Weiss syndrome
Sanger
1096 Crouzon syndrome with acanthosis nigricans
Sanger
1094 Crouzon syndrome
Sanger
1093 Craniosynostosis, type 1
Del Dup
1092 Craniosynostosis, type 1
Sanger
1091 Beare-Stevenson cutis gyrata syndrome
Sanger
1088 Apert syndrome
Sanger
1087 Craniometaphyseal dysplasia, autosomal dominant
NGS
1086 Cranioectodermal dysplasia 4
Del Dup
1085 Cranioectodermal dysplasia 4
NGS
1084 Cranioectodermal dysplasia 2
Del Dup
1083 Cranioectodermal dysplasia 2
NGS

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