Browse CTGT's catalogue of connective tissue tests, including NGS panels, by gene.
Extended Carrier Screening panel |
Atrioventricular block NGS Panel | |
Brugada syndrome and related disorders NGS panel | |
Extended Carrier Screening panel | |
Limb girdle muscular dystrophy NGS panel |
Extended Carrier Screening panel |
Extended Carrier Screening panel |
Extended Carrier Screening panel |
Mucopolysaccharidosis NGS panel |
Hyperphosphatemic familial tumoral calcinosis - GALNT3 | |
Hyperphosphatemic familial tumoral calcinosis NGS panel |
Extended Carrier Screening panel |
Extended Carrier Screening panel |
Distal hereditary motor neuropathy and related disorders NGS panel |
Polycystic kidney disease and related disorders NGS panel | |
Polycystic liver disease NGS panel |
Charcot-Marie-Tooth disease NGS panel | |
Distal hereditary motor neuropathy and related disorders NGS panel |
Diamond-Blackfan anemia NGS panel | |
Thrombocytopenia NGS Panel |
Vascular malformations NGS panel |
Congenital heart disease NGS panel |
Atrial fibrillation NGS panel | |
Congenital heart disease NGS panel |
Extended Carrier Screening panel |
Common Carrier Screening Panel | |
Extended Carrier Screening panel | |
Platelet bleeding disorders NGS panel | |
Thrombocytopenia NGS Panel |
Charcot-Marie-Tooth disease NGS panel |
Congenital heart disease NGS panel |
Hereditary Hemorrhagic telangiectasia NGS panel | |
Hereditary hemorrhagic telangiectasia type 5 | |
Pulmonary hypertension NGS panel | |
Vascular malformations NGS panel |
Klippel-Feil syndrome 3 | |
Klippel-Feil syndrome NGS panel |
Acromesomelic dysplasia, Hunter-Thompson type | |
Chondrodysplasia, Grebe type | |
Fibular hypoplasia and complex brachydactyly |
Klippel-Feil Syndrome 1 | |
Klippel-Feil syndrome NGS panel | |
Leber congenital amaurosis and related disorders NGS panel |
Platelet bleeding disorders NGS panel |
Pseudoxanthoma elasticum NGS panel | |
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency |
Short stature with endocrinopathy NGS panel |
Short stature with endocrinopathy NGS panel |
Short stature with endocrinopathy NGS panel |
Short stature with endocrinopathy NGS panel |
Dense bone dysplasia NGS panel | |
Erythrokeratodermias and related disorders NGS panel | |
Ichthyosis NGS panel | |
Oculodentodigital dysplasia | |
Osteopetrosis and Dense bone dysplasia NGS panel |
Atrial fibrillation NGS panel |
Charcot-Marie-Tooth disease NGS panel | |
Distal hereditary motor neuropathy and related disorders NGS panel |
Erythrokeratodermias and related disorders NGS panel | |
Ichthyosis NGS panel |
Erythrokeratodermias and related disorders NGS panel | |
Ichthyosis NGS panel |
Ectodermal dysplasia NGS panel |
Mucopolysaccharidosis NGS panel |
Congenital contracture syndrome extended NGS panel | |
Lethal congenital contracture syndrome and related disorders NGS Panel |
Congenital contracture syndrome extended NGS panel | |
Lethal congenital contracture syndrome and related disorders NGS Panel |
Craniosynostosis NGS panel | |
Greig cephalopolysyndactyly syndrome | |
Pallister-Hall syndrome | |
Polydactyly, preaxial IV & postaxial, type A1 |
Nephronophthisis and related disorders NGS panel |
Polycystic kidney disease and related disorders NGS panel |
Glomuvenous malformations | |
Glomuvenous malformations and Cutaneomucosal venous malformations NGS panel | |
Vascular malformations NGS panel |
Meier-Gorlin syndrome NGS panel | |
Microcephalic primordial dwarfism NGS panel |
Limb girdle muscular dystrophy NGS panel | |
Lissencephaly and related disorders NGS panel |
Bartter syndrome and related disorders NGS panel | |
Nephrolithiasis and related disorders NGS panel |
Auriculocondylar syndrome NGS panel |
Charcot-Marie-Tooth disease NGS panel |
Distal Myopathy NGS panel |
Chondrodysplasia punctata and related disorders NGS panel | |
Rhizomelic chondrodysplasia punctata, type 2 |
Mucopolysaccharidosis NGS panel |
Mucopolysaccharidosis NGS panel |
Mucopolysaccharidosis NGS panel |
Platelet bleeding disorders NGS panel |
Platelet bleeding disorders NGS panel |
Platelet bleeding disorders NGS panel |
Platelet bleeding disorders NGS panel |
Overgrowth syndrome NGS panel | |
Simpson-Golabi-Behmel syndrome, type 1 |
Omodysplasia NGS panel |
Brugada syndrome and related disorders NGS panel | |
Cardiac channelopathy NGS panel |
Amelogenesis imperfecta and related disorders NGS panel |
Spondylo-Epi-Metaphyseal dysplasias NGS panel |
Cleft lip, cleft palate and related disorders NGS panel | |
Van der Woude syndrome 2 | |
Van der Woude syndrome NGS panel |
Nephrolithiasis and related disorders NGS panel |
Trichothiodystrophy NGS panel |
Trichothiodystrophy NGS panel |
Leber congenital amaurosis and related disorders NGS panel |
Mucopolysaccharidosis NGS panel |
Desbuquois dysplasia and related disorders NGS panel |