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 Toluene embryopathy Methimazole embryofetopathy Cranioectodermal dysplasia Pierre Robin syndrome associated with collagen disease Non-syndromic bilambdoid and sagittal craniosynostosis Diabetic embryopathy Cantú syndrome Pierre Robin syndrome associated with a chromosomal anomaly Teebi-Shaltout syndrome Frontofacionasal dysplasia Rare disease with Pierre Robin syndrome SPECC1L-related hypertelorism syndrome Isolated oxycephaly Carpenter syndrome Craniofrontonasal dysplasia Autosomal recessive Stickler syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Oculomaxillofacial dysostosis 22q11.2 deletion syndrome TARP syndrome Fetal parvovirus syndrome Craniomicromelic syndrome Pierre Robin syndrome associated with branchial archs anomalies Isolated cloverleaf skull syndrome Oculoauriculofrontonasal syndrome 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 Dysplasie frontonasale acromélique Trouble rare de la succion/déglutition Syndrome de cutis gyrata-acanthosis nigricans-craniosynostose Syndrome de Goodman Syndrome de Cornelia de Lange Syndrome de dysplasie frontonasale-alopécie-anomalies génitales Syndrome de Crouzon Syndrome de Summitt Syndrome de dysplasie frontonasale-microphtalmie sévère-fente faciale sévère Dysplasie cranio-lenticulo-suturale Dysplasie de Kniest Syndrome de Muenke Syndrome C Syndrome d'Antley-Bixler Syndrome de Pai Syndrome d'Apert Maladie néoplasique rare Syndrome de craniosynostose-calcifications intracrâniennes Syndrome de Stickler 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