SE-ATLAS

Versorgungsatlas für Menschen mit seltenen Erkrankungen


Nachfolgend finden Sie die Erkrankungen, die in dieser Einrichtung behandelt werden:
48,XXXY-Syndrom 48,XXYY syndrome 48,XYYY syndrome 49,XXXXY-Syndrom ARX-related encephalopathy-brain malformation spectrum Abruzzo-Erickson syndrome Autosomal recessive faciodigitogenital syndrome Bladder exstrophy Branchioskeletogenital syndrome Caudal regression-sirenomelia spectrum Cloacal exstrophy Czeizel-Losonci-Syndrom Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome Exstrophy-epispadias complex Fehlbildung des Urogenitaltraktes, nicht-syndromale Fehlbildung des Urogenitaltraktes, syndromale Guttmacher syndrome Hypertelorism-hypospadias-polysyndactyly syndrome Hypospadias-intellectual disability, Goldblatt type syndrome IMAGe syndrome Isolated epispadias Juberg-Marsidi-Syndrom Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Lethal hemolytic anemia-genital anomalies syndrome Lower limb malformation-hypospadias syndrome Mikrodeletionssyndrom 8p23.1 Myopathy-growth delay-intellectual disability-hypospadias syndrome Müllerian duct anomalies-limb anomalies syndrome Nephrosis-deafness-urinary tract-digital malformations syndrome Non-syndromic urogenital tract malformation of female Non-syndromic urogenital tract malformation of male Non-syndromic urogenital tract malformation of male and female Opitz GBBB syndrome Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome Schilbach-Rott syndrome Spina bifida-hypospadias syndrome Torticollis-keloids-cryptorchidism-renal dysplasia syndrome Turner syndrome Urogenital tract malformation Uterusverdoppelung - Hemivagina - Nierenagenesie pondylokostale Dysostose-Analatresie-Urogenitalfehlbildung-Syndrom