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 syndrome Bifid uvula Orofaciodigital syndrome type 1 Orofaciodigital syndrome type 6 Pseudoaminopterin syndrome Orofaciodigital syndrome Osteosclerosis-developmental delay-craniosynostosis syndrome Crouzon syndrome Isolated encephalocele Cranioectodermal dysplasia SPECC1L-related hypertelorism syndrome SIX2-related frontonasal dysplasia Craniosynostosis, Philadelphia type Frontonasal dysplasia Otomandibular dysplasia FGFR2-related bent bone dysplasia Frontofacionasal dysplasia Cardiocranial syndrome, Pfeiffer type Nasal encephalocele Hunter-McAlpine syndrome Oculoauriculofrontonasal syndrome Acrodysostosis with multiple hormone resistance Oral-facial-digital syndrome with short stature and brachymesophalangy Townes-Brocks syndrome Orofaciodigital syndrome type 5 Autosomal recessive Stickler syndrome Non-syndromic craniosynostosis Cleft lip/palate Cleft hard palate Craniofaciofrontodigital syndrome Orofaciodigital syndrome type 10 Pfeiffer syndrome Baller-Gerold syndrome Isolated Pierre Robin syndrome Isolated oxycephaly Teebi-Shaltout syndrome Cleft palate Craniofrontonasal dysplasia Pfeiffer syndrome type 2 Pfeiffer syndrome type 1 Pfeiffer syndrome type 3 Otomandibular syndrome Antley-Bixler syndrome Apert syndrome Mandibulofacial dysostosis with alopecia Craniosynostosis, Herrmann-Opitz type Lowry-MacLean syndrome Holoprosencephaly-craniosynostosis syndrome Acrocephalopolydactyly Summitt syndrome Acrocephalosyndactyly Cleft velum Orofaciodigital syndrome type 3 Familial lambdoid synostosis Orofaciodigital syndrome type 8 Pai syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Familial osteodysplasia, Anderson type Carpenter syndrome Cantú syndrome Craniosynostosis-dental anomalies Oculoauriculovertebral spectrum with radial defects Craniosynostosis-fibular aplasia syndrome