SE-ATLAS

22q11.2 deletion syndrome Adult hypophosphatasia Albright hereditary osteodystrophy Aminopterin/methotrexate embryofetopathy Apert syndrome Atelosteogenesis type I Atelosteogenesis type II Atelosteogenesis type III Autosomal dominant otospondylomegaepiphyseal dysplasia Autosomal recessive Stickler syndrome Bifid nose Bone dysplasia, Azouz type Childhood-onset hypophosphatasia Cocaine embryofetopathy Coloboma of inferior eyelid Coloboma of superior eyelid Cornelia de Lange syndrome Crouzon syndrome Diabetic embryopathy Duchenne and Becker muscular dystrophy Facial cleft Familial median cleft of the upper and lower lips Fetal alcohol syndrome Fetal hydantoin syndrome Fetal iodine syndrome Fetal methylmercury syndrome Fetal minoxidil syndrome Fetal parvovirus syndrome Fetal trimethadione syndrome Fetal valproate spectrum disorder Frontofacionasal dysplasia Frontorhiny Goldenhar syndrome Hashimoto-Pritzker syndrome Hypophosphatasia Indomethacin embryofetopathy Infantile hypophosphatasia Intellectual disability-brachydactyly-Pierre Robin syndrome Isotretinoin syndrome Juvenile Paget disease Kabuki syndrome Kniest dysplasia Lateral facial cleft Maternal phenylketonuria Median cleft lip/mandible Median cleft of the upper lip and maxilla Median facial cleft Methimazole embryofetopathy Midline cervical cleft Multiple osteochondromas Nager syndrome Oblique facial cleft Odontohypophosphatasia Oligodontia Ollier disease Osteogenesis imperfecta Osteogenesis imperfecta type 1 Osteogenesis imperfecta type 2 Osteogenesis imperfecta type 3 Osteogenesis imperfecta type 4 Osteogenesis imperfecta type 5 Paramedian facial cleft Paramedian nasal cleft Perinatal lethal hypophosphatasia Phenobarbital embryopathy Pierre Robin syndrome associated with a chromosomal anomaly Pierre Robin syndrome associated with bone disease Pierre Robin syndrome associated with branchial archs anomalies Pierre Robin syndrome associated with collagen disease Pituitary gigantism Prenatal benign hypophosphatasia Pseudohypoparathyroidism type 1A Pseudohypoparathyroidism type 1C Pseudopseudohypoparathyroidism Rare disease with Pierre Robin syndrome Rare maxillo-facial surgical disease Rare odontologic disease Rare sucking/swallowing disorder Smith-Lemli-Opitz syndrome Smith-Magenis syndrome Stickler syndrome Stickler syndrome type 1 Stickler syndrome type 2 TARP syndrome Taurodontism Teratogenic Pierre Robin syndrome Tessier number 4 facial cleft Tessier number 5 facial cleft Tessier number 6 facial cleft Tessier number 7 facial cleft Toluene embryopathy Treacher-Collins syndrome Ulbright-Hodes syndrome Vitamin K antagonist embryofetopathy Waardenburg syndrome