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:
ADULT syndrome Adult hypophosphatasia Amelocerebrohypohidrotic syndrome Amelogenesis imperfecta Amelogenesis imperfecta-gingival hyperplasia syndrome Amelogenesis imperfecta-nephrocalcinosis syndrome Anodontia Atypical dentin dysplasia due to SMOC2 deficiency Autosomal dominant trichoodontoonychodysplasia-syndactyly Blepharo-cheilo-odontic syndrome Brachyolmia-amelogenesis imperfecta syndrome Bruck syndrome Cherubism Childhood-onset hypophosphatasia Cleft palate-stapes fixation-oligodontia syndrome Cleidocranial dysplasia Deafness-enamel hypoplasia-nail defects syndrome Deafness-oligodontia syndrome Dental ankylosis Dentin dysplasia Dentin dysplasia type I Dentin dysplasia type II Dentin dysplasia-sclerotic bones syndrome Dentinogenesis imperfecta Dentinogenesis imperfecta type 2 Dentinogenesis imperfecta type 3 Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome Dermoodontodysplasia Ectodermal dysplasia with natal teeth, Turnpenny type Ectodermal dysplasia, trichoodontoonychial type Ehlers-Danlos syndrome due to tenascin-X deficiency Ehlers-Danlos syndrome type 1 Ehlers-Danlos syndrome type 2 Ehlers-Danlos syndrome, classic type Ehlers-Danlos syndrome, periodontitis type Epidermolysis bullosa simplex with anodontia/hypodontia Florid cemento-osseous dysplasia Fused mandibular incisors GAPO syndrome Gingival fibromatosis-facial dysmorphism syndrome Gingival fibromatosis-hypertrichosis syndrome Haim-Munk syndrome Hereditary dentin defect Hereditary gingival fibromatosis Hypocalcified amelogenesis imperfecta Hypodontia-dysplasia of nails syndrome Hypomaturation amelogenesis imperfecta Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism Hypoplastic amelogenesis imperfecta Infantile hypophosphatasia Jalili syndrome Junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Junctional epidermolysis bullosa, generalized intermediate Junctional epidermolysis bullosa, generalized severe Junctional epidermolysis bullosa, non-Herlitz type Junctional epidermolysis bullosa-pyloric atresia syndrome KBG syndrome Kein Name gefunden Kein Name gefunden LOC syndrome Lacrimoauriculodentodigital syndrome Late-onset junctional epidermolysis bullosa Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome Localized junctional epidermolysis bullosa, non-Herlitz type Malformation syndrome with odontal and/or periodontal component Malformative syndrome with dentinogenesis imperfecta Nance-Horan syndrome Non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome Oculocerebral hypopigmentation syndrome, Cross type Oculodental syndrome, Rutherfurd type Oculodentodigital dysplasia Oculofaciocardiodental syndrome Oculootodental syndrome Odonto-onycho dysplasia-alopecia syndrome Odonto-onycho-dermal dysplasia Odonto-tricho-ungual-digito-palmar syndrome Odontochondrodysplasia Odontohypophosphatasia Odontomatosis-aortae esophagus stenosis syndrome Odontomicronychial dysplasia Odontotrichomelic syndrome Oligodontia Osteogenesis imperfecta type 3 Osteogenesis imperfecta type 4 Otodental syndrome Papillon-Lefèvre syndrome Pilodental dysplasia-refractive errors syndrome Postaxial polydactyly-dental and vertebral anomalies syndrome Pyramidal molars-abnormal upper lip syndrome Ramon syndrome Rare disease with dentinogenesis imperfecta Rare disease with odontological manifestation Rare odontal or periodontal disorder Rare odontologic disease Regional odontodysplasia Schimke immuno-osseous dysplasia Schöpf-Schulz-Passarge syndrome Segmental odontomaxillary dysplasia Steatocystoma multiplex-natal teeth syndrome Steroid dehydrogenase deficiency-dental anomalies syndrome Taurodontia-absent teeth-sparse hair syndrome Taurodontism Tricho-dento-osseous syndrome Trichodental syndrome Trichodermodysplasia-dental alterations syndrome Trichodysplasia-amelogenesis imperfecta syndrome Trichoodontoonychial dysplasia Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia Zimmermann-Laband syndrome