SE-ATLAS

Mapping of Health Care Providers
for People with Rare Diseases


In the following you will find the diseases that are treated in this facility:
22q11.2 deletion syndrome Amelogenesis imperfecta Angioosteohypotrophic syndrome Apert syndrome Bifid uvula CHARGE syndrome Cherubism Choanal atresia Cleft hard palate Cleft lip and alveolus Cleft lip/palate Cleft palate Cleft velum Cleidocranial dysplasia Craniosynostosis Crouzon syndrome Cysts and fistulae of the face and oral cavity Dentin dysplasia Dentinogenesis imperfecta Diffuse lymphatic malformation Diffuse neonatal hemangiomatosis Ectodermal dysplasia syndrome Facial arteriovenous malformation Facial cleft Familial median cleft of the upper and lower lips Fibrous dysplasia of bone Frontonasal dysplasia GAPO syndrome Goldenhar syndrome Gorlin syndrome Hallermann-Streiff syndrome Hypoglossia/aglossia Isolated Pierre Robin syndrome Lateral facial cleft Macroglossia Mandibular arteriovenous malformation Mandibulofacial dysostosis Maxillary arteriovenous malformation Median cleft of the upper lip and maxilla Median facial cleft Moebius syndrome Nager syndrome Non-involuting congenital hemangioma Non-syndromic metopic craniosynostosis Non-syndromic sagittal craniosynostosis Noonan syndrome Oblique facial cleft Oligodontia Orofaciodigital syndrome Orofaciodigital syndrome type 2 Otomandibular syndrome Papillon-Lefèvre syndrome Paramedian facial cleft Pfeiffer syndrome Rapidly involuting congenital hemangioma Rare arteriovenous malformation Rare lymphatic malformation Rare venous malformation Saethre-Chotzen syndrome Seckel syndrome Tessier number 7 facial cleft Treacher-Collins syndrome Van der Woude syndrome