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:
17q11 microdeletion syndrome Acanthokeratolytic verrucous nevus Adult T-cell leukemia/lymphoma Aggressive primary cutaneous B-cell lymphoma Aggressive primary cutaneous T-cell lymphoma Angora hair nevus Bannayan-Riley-Ruvalcaba syndrome Bazex-Dupré-Christol syndrome Becker nevus syndrome Birt-Hogg-Dubé syndrome Brooke-Spiegler syndrome CHILD syndrome CLAPO syndrome CLOVES syndrome Calcifying aponeurotic fibroma Congenital panfollicular nevus Congenital smooth muscle hamartoma Cowden syndrome Cutaneous neuroendocrine carcinoma Cystic hygroma Dermatofibrosarcoma protuberans Didymosis aplasticosebacea Diffuse lymphatic malformation Epidermal nevus syndrome Extranodal nasal NK/T cell lymphoma Familial cylindromatosis Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Familial keratoacanthoma Familial melanoma Familial multiple fibrofolliculoma Familial multiple trichoepithelioma Familial normophosphatemic tumoral calcinosis Familial tumoral calcinosis Follicular atrophoderma-basal cell carcinoma Gardner syndrome Generalized basaloid follicular hamartoma syndrome Gorlin syndrome Granulomatous slack skin Hemihyperplasia-multiple lipomatosis syndrome Hereditary leiomyomatosis and renal cell cancer Indolent primary cutaneous B-cell lymphoma Indolent primary cutaneous T-cell lymphoma Infantile digital fibromatosis Infantile myofibromatosis Inflammatory linear verrucous epidermal nevus Large congenital melanocytic nevus Ledderhose disease Linear nevus sebaceus syndrome Linear verrucous nevus syndrome Macrocystic lymphatic malformation Malignant melanoma of the mucosa Microcystic lymphatic malformation Muir-Torre syndrome Multiple self-healing squamous epithelioma Mycosis fungoides and variants NEVADA syndrome Neurocutaneous melanocytosis Neurofibromatosis type 1 Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Nevus comedonicus syndrome Nevus of Ito Nevus of Ota Oley syndrome Onychocytic matricoma Onychomatricoma PENS syndrome PTEN hamartoma tumor syndrome Phakomatosis pigmentokeratotica Pilomatrixoma Porokeratotic eccrine ostial and dermal duct nevus Primary cutaneous B-cell lymphoma Primary cutaneous CD30+ T-cell lymphoproliferative disease Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Primary cutaneous T-cell lymphoma Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Primary cutaneous diffuse large B-cell lymphoma, leg type Primary cutaneous follicle center lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Primary cutaneous lymphoma Primary cutaneous marginal zone B-cell lymphoma Primary cutaneous peripheral T-cell lymphoma not otherwise specified Proliferating trichilemmal cyst Proteus syndrome Proteus-like syndrome Rare lymphatic malformation Rare nail tumor Rare nevus Rare skin tumor or hamartoma Rombo syndrome SCALP syndrome Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Subcutaneous panniculitis-like T-cell lymphoma Superficial fibromatosis Syringocystadenoma papilliferum Sézary syndrome Trichofolliculoma Verrucous nevus White sponge nevus