SE-ATLAS

Rare nail tumor Muir-Torre syndrome Trichofolliculoma Nevus of Ota Generalized basaloid follicular hamartoma syndrome CLOVES syndrome Nevus of Ito Proteus syndrome Cowden syndrome Familial multiple fibrofolliculoma Congenital smooth muscle hamartoma Extramammary Paget disease Epidermal nevus syndrome Familial melanoma Oley syndrome Large congenital melanocytic nevus Proliferating trichilemmal cyst Hemihyperplasia-multiple lipomatosis syndrome Familial keratoacanthoma Gorlin syndrome Granulomatous slack skin Proteus-like syndrome PENS syndrome Becker nevus syndrome Nevus comedonicus syndrome Rombo syndrome Bazex-Dupré-Christol syndrome Hereditary leiomyomatosis and renal cell cancer Brooke-Spiegler syndrome Familial tumoral calcinosis Birt-Hogg-Dubé syndrome Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Superficial fibromatosis Primary cutaneous lymphoma Infantile myofibromatosis Subcutaneous panniculitis-like T-cell lymphoma Rare nevus CHILD syndrome Angora hair nevus White sponge nevus Generalized eruptive keratoacanthoma Multiple selbstheilende squamöse Epitheliome Hauttumor oder Hamartom, seltene Formen Malignes Melanom der Mukosa Phakomatosis pigmento-keratotica Didymosis aplasticosebacea Gardner-Syndrom Dermatofibrosarcoma protuberans Syndrom des linearen verrukösen Naevus Syndrom des linearen Naevus sebaceus Syringocystadenoma papilliferum PTEN-Hamartom-Tumor-Syndrom Naevus, panfollikulärer, kongenitaler SCALP-Syndrom Melanozytose, neurokutane Familiäres atpisches multiples Muttermal- und Melanomsyndrom Ostiumnaevus, ekkriner porokeratotischer Karzinom, kutanes neuroendokrines Pilomatrixom NEVADA-Syndrom