SE-ATLAS

Hypomaturation amelogenesis imperfecta Hypocalcified amelogenesis imperfecta Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism Ehlers-Danlos syndrome Myopathic Ehlers-Danlos syndrome Dentinogenesis imperfecta Kyphoscoliotic Ehlers-Danlos syndrome due to FKBP22 deficiency Classical-like Ehlers-Danlos syndrome type 2 Spondylodysplastic Ehlers-Danlos syndrome B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome Brittle cornea syndrome Hypoplastic amelogenesis imperfecta Cardiac-valvular Ehlers-Danlos syndrome Periodontal Ehlers-Danlos syndrome Vascular Ehlers-Danlos-polymicrogyria syndrome Musculocontractural Ehlers-Danlos syndrome SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome Amelogenesis imperfecta B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Vascular Ehlers-Danlos syndrome X-linked Ehlers-Danlos syndrome Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency Dentinogenesis imperfecta type 2 Hypermobile Ehlers-Danlos syndrome Papillon-Lefèvre syndrome Arthrochalasia Ehlers-Danlos syndrome Classical-like Ehlers-Danlos syndrome type 1 Classical Ehlers-Danlos syndrome Kyphoscoliotic Ehlers-Danlos syndrome Dermatosparaxis Ehlers-Danlos syndrome Dentinogenesis imperfecta type 3