Connective Tissue Gene Tests
Contact Us
(484) 244-2900
About
About Us
Why Use CTGT
Our Experts
Contact Us
CTGT Licenses
Terms Of Use
Methods
Turnaround Time
Tests
By Disorder
By Gene
By Disease Group
By Test Code
By Panel
New Tests
Carrier Screening
New York State Testing
Order
How to Order
Requisition Form
Specimens
Shipping
Billing & Payments
Add-On Tests
Prenatal Tests
Targeted and VUS Testing
Prices & CPT Codes
For Patients
News & Events
News
Events
Test Catalogue by Test Code
Disorder
Gene
Disease Group
Test Code
Panel
Browse CTGT's test catalogue, including NGS panels, by test code.
Test Code
Disorder / Panel Name
Test Code
Disorder or Panel
Test Method
1053
Avascular necrosis of femoral head, primary
NGS
1059
Bethlem myopathy & Ullrich congenital muscular dystrophy NGS panel
NGS
1060
Boomerang dysplasia
NGS
1061
Boomerang dysplasia
Sanger
1063
Brachyolmia type 3
NGS
1064
Brittle cornea syndrome 1
NGS
1065
Brittle cornea syndrome 1
Del Dup
1066
Brittle cornea syndrome 2
NGS
1067
Brittle cornea syndrome 2
Del Dup
1068
Bruck syndrome 2
NGS
1069
Buschke-Ollendorff syndrome
NGS
1070
Buschke-Ollendorff syndrome
Del Dup
1071
Caffey disease
NGS
1072
Campomelic dysplasia
NGS
1073
Campomelic dysplasia
Del Dup
1074
Camurati-Engelmann disease
NGS
1075
Capillary malformation arteriovenous malformation
NGS
1076
Capillary malformation arteriovenous malformation
Del Dup
1077
Cardiac valvular dysplasia, X-linked
NGS
1078
Cartilage-hair hypoplasia
Sanger
1079
Chondrocalcinosis 2
NGS
1080
Cleidocranial dysplasia
NGS
1081
Congenital contractural arachnodactyly
NGS
1082
Congenital contractural arachnodactyly
Del Dup
1083
Cranioectodermal dysplasia 2
NGS
1084
Cranioectodermal dysplasia 2
Del Dup
1085
Cranioectodermal dysplasia 4
NGS
1086
Cranioectodermal dysplasia 4
Del Dup
1087
Craniometaphyseal dysplasia, autosomal dominant
NGS
1088
Apert syndrome
Sanger
1091
Beare-Stevenson cutis gyrata syndrome
Sanger
1092
Craniosynostosis, type 1
Sanger
1093
Craniosynostosis, type 1
Del Dup
1094
Crouzon syndrome
Sanger
1096
Crouzon syndrome with acanthosis nigricans
Sanger
1097
Jackson-Weiss syndrome
Sanger
1098
Muenke syndrome
Sanger
1099
Pfeiffer syndrome
Sanger
1101
Saethre-Chotzen syndrome
Sanger
1102
Saethre-Chotzen syndrome
Del Dup
1103
FGFR1, FGFR2 and FGFR3 related craniosynostosis panel
Sanger
1104
FGFR1, FGFR2, FGFR3 & TWIST1 related craniosynostosis panel
Sanger
1105
FGFR2 related craniosynostosis
NGS
1106
FGFR2 related craniosynostosis
Del Dup
1107
Cutis laxa, autosomal dominant 2 & autosomal recessive, type IA
NGS
1108
Cutis laxa, autosomal dominant 2 & autosomal recessive, type IA
Del Dup
1109
Cutis laxa, autosomal recessive 1B
NGS
1110
Cutis laxa, autosomal recessive 1B
Del Dup
1111
Cutis laxa, autosomal recessive 1A
Sanger
1112
Cutis laxa, autosomal recessive 1A
Del Dup
Pages
« first
‹ previous
1
2
3
4
5
6
7
…
next ›
last »
Search Tests
Enter a disorder, gene, or test code
TIP: enter a partial disorder name or gene to widen your search
Browse Tests By
Disorder
Gene
Disease Group
Test Code
Panel
Order Tests
How to Order
Requisition Form & Instructions
Specimens
Shipping
Billing & Payments
Prices & CPT Codes
Quick Links
Test Requisition Form
Shipment Packing Slip
Prior Authorization Information packet