Browse CTGT's catalogue of connective tissue tests, including NGS panels, by gene.
| Limb girdle muscular dystrophy NGS panel |
| Mucopolysaccharidosis NGS panel |
| Hyperphosphatemic familial tumoral calcinosis - GALNT3 | |
| Hyperphosphatemic familial tumoral calcinosis NGS panel |
| Distal hereditary motor neuropathy and related disorders NGS panel |
| Charcot-Marie-Tooth disease NGS panel | |
| Distal hereditary motor neuropathy and related disorders NGS panel |
| Thrombocytopenia NGS Panel |
| Vascular malformations NGS panel |
| Congenital heart disease NGS panel |
| Congenital heart disease NGS panel |
| Charcot-Marie-Tooth disease NGS panel |
| Congenital heart disease NGS panel |
| Hereditary Hemorrhagic telangiectasia NGS panel | |
| Hereditary hemorrhagic telangiectasia type 5 | |
| 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 |
| Platelet bleeding disorders NGS panel |
| Pseudoxanthoma elasticum NGS panel | |
| Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency |
| Dense bone dysplasia NGS panel | |
| Ichthyosis NGS panel - Nonsyndromic | |
| Oculodentodigital dysplasia | |
| Osteopetrosis and Dense bone dysplasia NGS panel |
| Charcot-Marie-Tooth disease NGS panel | |
| Distal hereditary motor neuropathy and related disorders NGS panel |
| Ichthyosis NGS panel - Nonsyndromic |
| Ichthyosis NGS panel - Nonsyndromic |
| Ectodermal dysplasia NGS panel |
| Mucopolysaccharidosis NGS panel |
| Craniosynostosis NGS panel | |
| Greig cephalopolysyndactyly syndrome | |
| Pallister-Hall syndrome | |
| Polydactyly, preaxial IV & postaxial, type A1 |
| 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 |
| Charcot-Marie-Tooth disease NGS panel |
| Distal Myopathy |
| 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 |
| Simpson-Golabi-Behmel syndrome | |
| Simpson-Golabi-Behmel, Sotos and Weaver syndrome NGS panel |
| Omodysplasia 1 |
| Amelogenesis imperfecta and related disorders NGS panel |
| Spondylo-Epi-Metaphyseal dysplasias NGS panel |
| Van der Woude syndrome 1 / 2 | |
| Van der Woude syndrome 2 |
| Mucopolysaccharidosis NGS panel |