Browse CTGT's catalogue of connective tissue tests, including NGS panels, by gene.

DAG1
Limb girdle muscular dystrophy NGS panel
Del Dup
NGS
DCAF8
Distal hereditary motor neuropathy and related disorders NGS panel
Del Dup
NGS
DCHS1
Mitral valve prolapse 2
Del Dup
NGS
Van Maldergem syndrome 1
Del Dup
NGS
DCTN1
Distal hereditary motor neuropathy and related disorders NGS panel
NGS
Del Dup
DDR2
Skeletal dysplasia core & extended NGS panel
Del Dup
NGS
Skeletal dysplasia extended NGS panel
Del Dup
NGS
Spondylo-Epi-Metaphyseal dysplasias NGS panel
Del Dup
NGS
DES
Distal Myopathy
Del Dup
NGS
Limb girdle muscular dystrophy NGS panel
Del Dup
NGS
Myofibrillar myopathy and related disorders NGS panel
Del Dup
NGS
DGKE
Atypical hemolytic uremic syndrome susceptibility and related disorders NGS panel
Del Dup
NGS
Nephrotic syndrome and related disorders NGS panel
NGS
Del Dup
DHCR7
Smith-Lemli-Opitz syndrome
Sanger
Del Dup
DHODH
Postaxial acrofacial dysostosis
Del Dup
Sanger
Treacher Collins syndrome and related disorders NGS panel
Del Dup
NGS
DHTKD1
Charcot-Marie-Tooth disease NGS panel
NGS
Del Dup
DKC1
Dyskeratosis congenita NGS panel
NGS
Del Dup
DLL3
Spondylocostal dysostosis 1, autosomal recessive
Del Dup
Sanger
Spondylocostal dysostosis NGS panel
Del Dup
NGS
DLL4
Adams-Oliver syndrome 6
NGS
Del Dup
Adams-Oliver syndrome NGS panel
NGS
Del Dup
DLX3
Amelogenesis imperfecta and related disorders NGS panel
Del Dup
NGS
Amelogenesis imperfecta, type IV
Del Dup
Sanger
Dense bone dysplasia NGS panel
NGS
Del Dup
Osteopetrosis and Dense bone dysplasia NGS panel
Del Dup
NGS
Trichodentoosseus syndrome
Del Dup
Sanger
DMP1
Abnormal mineralization disorders NGS panel
Del Dup
NGS
Rickets, hypophosphatemic, autosomal recessive, 1
Del Dup
NGS
DNA2
Microcephalic primordial dwarfism NGS panel
Del Dup
NGS
DNAJB2
Distal hereditary motor neuropathy and related disorders NGS panel
NGS
Del Dup
DNAJB6
Distal Myopathy
NGS
Del Dup
Limb girdle muscular dystrophy NGS panel
Del Dup
NGS
Myofibrillar myopathy and related disorders NGS panel
NGS
Del Dup
DNM2
Charcot-Marie-Tooth disease NGS panel
NGS
Del Dup
Distal Myopathy
Del Dup
NGS
DOCK6
Adams-Oliver syndrome 2
Del Dup
NGS
Adams-Oliver syndrome NGS panel
Del Dup
NGS
DSE
Ehlers-Danlos syndrome NGS panel - Dominant & Recessive
NGS
Del Dup
Ehlers-Danlos syndrome NGS panel - Recessive
Del Dup
NGS
DSP
Epidermolysis bullosa NGS panel
Del Dup
NGS
DSPP
Amelogenesis imperfecta and related disorders NGS panel
Del Dup
NGS
DST
Epidermolysis bullosa NGS panel
Del Dup
NGS
DTNBP1
Platelet bleeding disorders NGS panel
Del Dup
NGS
DVL1
Robinow syndrome NGS panel
NGS
Del Dup
Robinow syndrome, autosomal dominant 2
Sanger
Del Dup
DVL3
Robinow syndrome NGS panel
Del Dup
NGS
DYM
Dyggve-Melchior-Clausen disease
NGS
Del Dup
Smith-McCort dysplasia
NGS
Del Dup
Spondylo-Epi-Metaphyseal dysplasias NGS panel
NGS
Del Dup
DYNC1H1
Charcot-Marie-Tooth disease NGS panel
NGS
Del Dup
Distal hereditary motor neuropathy and related disorders NGS panel
NGS
Del Dup
DYNC2H1
Short-rib thoracic dysplasia 3 with or without polydactyly
Del Dup
NGS
Skeletal dysplasia ciliopathy NGS panel
Del Dup
NGS
DYSF
Distal Myopathy
NGS
Del Dup
Limb girdle muscular dystrophy NGS panel
NGS
Del Dup

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