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 Pierre Robin syndrome associated with bone disease Dysostosis with predominant craniofacial involvement Craniosynostosis, Philadelphia type Maternal phenylketonuria Craniotelencephalic dysplasia Pfeiffer syndrome Frontorhiny Teratogenic Pierre Robin syndrome Craniosynostosis-cataract syndrome Waardenburg syndrome Craniosynostosis Pseudoaminopterin syndrome Craniosynostosis-fibular aplasia syndrome Maternal hyperthermia-induced birth defects X-linked intellectual disability-plagiocephaly syndrome Kraniosynostose - Dysmorphien - Brachydaktylie Pierre-Robin-Sequenz, isolierte Kraniosynostose - Dandy-Walker-Malformation - Hydrozephalus Skaphokephalie-Syndrom, familiäres Jackson-Weiss-Syndrom Kraniosynostose Typ Boston Sagittalnaht-Synostose, nicht-syndromale Osteodysplasie, familiäre, Typ Anderson Kraniosynostose und Zahnanomalien Skaphozephalie-Syndrom, familiäres, Typ McGillivray Treacher-Collins-Syndrom Plagiozephalie, isolierte Synostose, bikoronare, nicht-syndromale Kleeblattschädel - asphyxierende Thoraxdysplasie Curry-Jones-Syndrom Dysplasie, akromele frontonasale Saug-/Schluckstörung Cutis gyrata-Acanthosis nigricans-Kraniosynostose-Syndrom Goodman-Syndrom Cornelia de Lange-Syndrom Fronto-nasale Dysplasie mit Alopezie und Genitalanomalien Crouzon-Syndrom Summitt-Syndrom Fronto-nasale Dysplasie-schwere Mikrophthalmie-Gesichtsspalten-Syndrom Dysplasie, kranio-lentikulo-suturale Kniest-Dysplasie Muenke-Syndrom C-Syndrom Antley-Bixler-Syndrom Pai-Syndrom Apert-Syndrom Seltene neoplastische Krankheit Kraniosynostose-intrakranielle Kalzifizierung-Syndrom Stickler-Syndrom Typ 2 Mandibulofaziale Dysostose - Makroblepharon - Makrostomie Kranio-fazio-fronto-digitales Syndrom Fragiles X-Syndrom Stickler-Syndrom Typ 1 Nebennierenhyperplasie, kongenitale, durch Cytochrom-P450-Oxydoreduktase-Mangel Lowry-Maclean-Syndrom Enzephalozele, frontonasale Trigonozephalie - breite Daumen Kraniosynostose-anale Anomalien-Porokeratose-Syndrom Kraniosynostose, metopische, nicht-syndromale Okulo-aurikulo-vertebrales Spektrum mit radialen Defekten Hunter-McAlpine -Syndrom Trigonozephalie - Kleinwuchs - Entwicklungsverzögerung Akrozephalopolydaktylie Atelosteogenesis Typ I Kraniosynostose Typ Herrmann-Opitz Multiple Synostosen