SE-ATLAS

Goldenhar syndrome Pfeiffer syndrome type 1 Pfeiffer syndrome type 3 Pfeiffer syndrome type 2 Crouzon syndrome-acanthosis nigricans syndrome Rare otorhinolaryngologic disease Nager syndrome Isolated encephalocele Autosomal dominant otospondylomegaepiphyseal dysplasia Osteosclerosis-developmental delay-craniosynostosis syndrome Atelosteogenesis type II Saethre-Chotzen syndrome Atelosteogenesis type III Cloverleaf skull-multiple congenital anomalies syndrome Frontonasal dysplasia Holoprosencephaly-craniosynostosis syndrome Isotretinoin syndrome Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Dobrow syndrome Acrocephalosyndactyly Familial lambdoid synostosis Non-syndromic craniosynostosis Fetal valproate spectrum disorder SCARF syndrome Baller-Gerold syndrome Rare maxillo-facial surgical disease Aminopterin/methotrexate embryofetopathy Syndromic craniosynostosis Indomethacin embryofetopathy Smith-Lemli-Opitz syndrome Intellectual disability-brachydactyly-Pierre Robin syndrome Fetal iodine syndrome Smith-Magenis syndrome Cocaine embryofetopathy Fetal hydantoin syndrome Kabuki syndrome Fetal trimethadione syndrome Vitamin K antagonist embryofetopathy Fetal alcohol syndrome Lethal occipital encephalocele-skeletal dysplasia syndrome Shprintzen-Goldberg syndrome Fetal methylmercury syndrome Cardiocranial syndrome, Pfeiffer type Fetal minoxidil syndrome Phenobarbital embryopathy Stickler syndrome Embryopathie au toluène Embryofoetopathie au méthimazole Dysplasie cranio-ectodermique Syndrome de Pierre Robin associée à une collagénopathie Craniosynostose bilambdoïde et sagittale non syndromique Embryopathie diabétique Syndrome de Cantú Syndrome de Pierre Robin associée à une anomalie chromosomique Syndrome de Teebi-Shaltout Dysplasie fronto-facio-nasale Maladie rare avec syndrome de Pierre Robin Syndrome d'hypertélorisme associé à SPECC1L Oxycéphalie isolée Syndrome de Carpenter Dysplasie cranio-fronto-nasale Syndrome de Stickler autosomique récessif Syndrome de dysplasie cranio-fronto-nasale-anomalie de Poland Dysostose oculo-maxillo-faciale Syndrome de délétion 22q11.2 Syndrome TARP Embryopathie à parvovirus Syndrome cranio-micromélique Syndrome de Pierre Robin associée à une anomalie des arcs branchiaux Crâne en trèfle isolé Syndrome oculo-auriculo-fronto-nasal Syndrome de Pierre Robin associée à une maladie osseuse Dysostose craniofaciale Craniosynostose type Philadelphie Phénylcétonurie maternelle Dysplasie cranio-télencéphalique Syndrome de Pfeiffer Frontorhinie Syndrome de Pierre Robin d'origine tératogène Syndrome de craniosynostose-cataracte Syndrome de Waardenburg Craniosynostose Syndrome pseudo-aminoptérine Syndrome de craniosynostose-aplasie du péroné Hyperthermie tératogène Syndrome de déficience intellectuelle liée à l'X-plagiocéphalie Syndrome de craniosynostose-brachydactylie Syndrome de Pierre Robin isolé Syndrome de craniosynostose-malformation de Dandy-Walker-hydrocéphalie Sacophocépalie syndromique familiale Syndrome de Jackson-Weiss Craniosynostose type Boston Craniosynostose sagittale non syndromique Ostéodysplasie familiale type Anderson Craniosynostose-anomalies dentaires Scaphocéphalie familiale type McGillivray Syndrome de Treacher-Collins Plagiocéphalie isolée Craniosynostose bicoronale non syndromique Syndrome de crâne en trèfle-dysplasie asphyxiante du thorax Syndrome de Curry-Jones Acromelic frontonasal dysplasia Rare sucking/swallowing disorder Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Goodman syndrome Cornelia de Lange syndrome Frontonasal dysplasia-alopecia-genital anomalies syndrome Crouzon syndrome Summitt syndrome Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome Craniolenticulosutural dysplasia Kniest dysplasia Muenke syndrome C syndrome Antley-Bixler syndrome Pai syndrome Apert syndrome Rare neoplastic disease Craniosynostosis-intracranial calcifications syndrome Stickler syndrome type 2 Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome Craniofaciofrontodigital syndrome Fragile X syndrome Stickler syndrome type 1 Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Lowry-MacLean syndrome Nasal encephalocele Trigonocephaly-broad thumbs syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Non-syndromic metopic craniosynostosis Oculoauriculovertebral spectrum with radial defects Hunter-McAlpine syndrome Trigonocephaly-short stature-developmental delay syndrome Acrocephalopolydactyly Atelosteogenesis type I Craniosynostosis, Herrmann-Opitz type Multiple synostoses syndrome