SE-ATLAS

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