SE-ATLAS

Oculomaxillofacial dysostosis Jackson-Weiss syndrome Craniosynostosis, Boston type Orofaciodigital syndrome type 14 Goodman syndrome Dysostosis with predominant craniofacial involvement Orofaciodigital syndrome type 12 Orofaciodigital syndrome type 13 Lambert syndrome Curry-Jones syndrome Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Occipital encephalocele Non-syndromic sagittal craniosynostosis Muenke syndrome Basal encephalocele Saethre-Chotzen syndrome Isolated plagiocephaly Non-syndromic bicoronal craniosynostosis C syndrome Stickler syndrome type 1 Parietal encephalocele Stickler syndrome type 2 Lethal occipital encephalocele-skeletal dysplasia syndrome Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome Acromelic frontonasal dysplasia Intellectual disability-brachydactyly-Pierre Robin syndrome Trigonocephaly-broad thumbs syndrome Frontonasal dysplasia-alopecia-genital anomalies syndrome Contractures-developmental delay-Pierre Robin syndrome Non-syndromic metopic craniosynostosis Isolated cloverleaf skull syndrome Frontorhiny 22q11.2 deletion syndrome Pierre Robin syndrome associated with collagen disease Stickler syndrome Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Rare disease with Pierre Robin syndrome Oculo-auriculo-vertebral spectrum Cloverleaf skull-multiple congenital anomalies syndrome Craniosynostosis-intracranial calcifications syndrome Treacher-Collins syndrome Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome Cloverleaf skull-asphyxiating thoracic dysplasia syndrome Syndromic craniosynostosis Frontal encephalocele Auriculocondylar syndrome Acrodysostosis Dobrow syndrome Orofaciodigital syndrome type 2 Orofaciodigital syndrome type 4 Familial scaphocephaly syndrome Orofaciodigital syndrome type 11 Orofaciodigital syndrome type 9 Submucosal cleft palate Non-syndromic bilambdoid and sagittal craniosynostosis Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Craniomicromelic syndrome Nager syndrome Craniotelencephalic dysplasia Mandibulofacial dysostosis Craniosynostosis-cataract syndrome Otomandibular dysplasia associated with monogenic syndromes Trigonocephaly-short stature-developmental delay syndrome Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome Pierre Robin syndrome associated with a chromosomal anomaly SCARF syndrome Pierre Robin syndrome associated with branchial archs anomalies Pierre Robin syndrome associated with bone disease TARP syndrome Teratogenic Pierre Robin syndrome Crouzon syndrome-acanthosis nigricans syndrome X-linked intellectual disability-plagiocephaly syndrome BOR syndrome Goldenhar syndrome Isolated cleft lip Weiss-Kruszka Syndrome Shprintzen-Goldberg-Syndrom Uvula bifida Oro-fazio-digitales Syndrom Typ 1 Oro-fazio-digitales Syndrom Typ 6 Pseudoaminopterin-Syndrom Oro-fazio-digitales Syndrom Osteosklerose-Entwicklungsverzögerung-Kraniosynostose-Syndrom Crouzon-Syndrom Enzephalozele, isolierte Dysplasie, kranioektodermale SPECC1L-assoziiertes Hypertelorismus-Syndrom SIX2-assoziierte frontonasale Dysplasie Kraniosynostose Typ Philadelphia Dysplasie, fronto-nasale Dysplasie, otomandibuläre FGFR2-abhängige Dysplasie mit gekrümmten Knochen Dysplasie, fronto-fazio-nasale Kardiokraniales Syndrom Typ Pfeiffer Enzephalozele, frontonasale Hunter-McAlpine -Syndrom Okulo-aurikulo-fronto-nasales Syndrom Akrodysostose mit multipler Hormonresistenz Oro-Fazio-Digitales Syndrom mit Kleinwuchs und Brachymesophalangie Townes-Brocks-Syndrom Oro-fazio-digitales Syndrom Typ 5 Stickler-Syndrom, autosomal-rezessives Kraniosynostose, nicht-syndromale Lippen-Kiefer-Gaumenspalte Spaltbildung des harten Gaumens Kranio-fazio-fronto-digitales Syndrom Oro-fazio-digitales Syndrom Typ 10 Pfeiffer-Syndrom Baller-Gerold-Syndrom Pierre-Robin-Sequenz, isolierte Oxyzephalie, isolierte Teebi-Shaltout-Syndrom Gaumenspalte Dysplasie, kranio-fronto-nasale Pfeiffer-Syndrom Typ 2 Pfeiffer-Syndrom Typ 1 Pfeiffer-Syndrom Typ 3 Mikrosomie, hemifaziale Antley-Bixler-Syndrom Apert-Syndrom Mandibulofaziale Dysostose mit Alopezie Kraniosynostose Typ Herrmann-Opitz Lowry-Maclean-Syndrom Holoprosenzephalie-Kraniosynostose-Syndrom Akrozephalopolydaktylie Summitt-Syndrom Akrozephalosyndaktylie Velumspalte Oro-fazio-digitales Syndrom Typ 3 Familiäre lambdoide Synostose Oro-fazio-digitales Syndrom Typ 8 Pai-Syndrom Kraniosynostose-anale Anomalien-Porokeratose-Syndrom Osteodysplasie, familiäre, Typ Anderson Carpenter-Syndrom Hypertrichose mit Osteochondrodysplasie vom Typ Cantú Kraniosynostose und Zahnanomalien Okulo-aurikulo-vertebrales Spektrum mit radialen Defekten Kraniosynostose -Fibula--Syndrom