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:
Acalvaria Adducted thumbs-arthrogryposis syndrome, Christian type Ankyloblepharon filiforme adnatum-imperforate anus syndrome Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Arthrogryposis multiplex congenita-whistling face syndrome Autosomal dominant popliteal pterygium syndrome BOR syndrome Beckwith-Wiedemann syndrome CHARGE syndrome Cantú syndrome Cleft palate Cleidocranial dysplasia Cranial malformation Craniodiaphyseal dysplasia Craniofaciofrontodigital syndrome Craniosynostosis Delayed membranous cranial ossification Dobrow syndrome Dysostosis with predominant craniofacial involvement EEC syndrome Enlarged parietal foramina Facial cleft Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome Familial osteodysplasia, Anderson type Frontonasal dysplasia Goldenhar syndrome Hypoglossia/aglossia Hypomandibular faciocranial dysostosis Isolated Pierre Robin syndrome Isolated ankyloblepharon filiforme adnatum Isolated congenital syngnathia Macroglossia Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome Marden-Walker syndrome Maxillonasal dysplasia Monosomy 18q Morgagni-Stewart-Morel syndrome Multiple pterygium-malignant hyperthermia syndrome Non-syndromic bilambdoid and sagittal craniosynostosis Oculoauriculovertebral spectrum with radial defects Oculomaxillofacial dysostosis Orofacial clefting syndrome Orofaciodigital syndrome Otomandibular dysplasia Otopalatodigital syndrome Popliteal pterygium syndrome Postaxial acrofacial dysostosis Proteus syndrome Rare disease with Pierre Robin syndrome Rare maxillo-facial surgical disease Simpson-Golabi-Behmel syndrome Simpson-Golabi-Behmel syndrome type 2 Syndrome or malformation associated with head and neck malformations Teebi-Shaltout syndrome Treacher-Collins syndrome Van den Ende-Gupta syndrome Van der Woude syndrome