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:
ANE syndrome Acanthokeratolytic verrucous nevus Acquired epidermolysis bullosa Acquired hypertrichosis lanuginosa Acral peeling skin syndrome Acral self-healing collodion baby Acromelanosis Adult T-cell leukemia/lymphoma Aggressive primary cutaneous B-cell lymphoma Aggressive primary cutaneous T-cell lymphoma Albinism-deafness syndrome Alopecia Alopecia antibody deficiency Alopecia totalis Alopecia universalis Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Alopecia-intellectual disability syndrome Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Angora hair nevus Annular epidermolytic ichthyosis Atrichia with papular lesions Autoimmune bullous skin disease Autoinflammatory syndrome with skin involvement Autosomal dominant epidermolytic ichthyosis Autosomal ichthyosis syndrome with fatal disease course Autosomal ichthyosis syndrome with other associated signs Autosomal ichthyosis syndrome with prominent hair abnormalities Autosomal ichthyosis syndrome with prominent neurologic signs Autosomal recessive congenital ichthyosis Bannayan-Riley-Ruvalcaba syndrome Barber-Say syndrome Bathing suit ichthyosis Bazex-Dupré-Christol syndrome Becker nevus syndrome Benign cephalic histiocytosis Birt-Hogg-Dubé syndrome Björnstad syndrome Brooke-Spiegler syndrome Bullous pemphigoid CEDNIK syndrome CHILD syndrome CLAPO syndrome CLOVES syndrome CREST syndrome Calcifying aponeurotic fibroma Cataract-hypertrichosis-intellectual disability syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Chédiak-Higashi syndrome Congenital generalized hypertrichosis, Ambras type Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Congenital non-bullous ichthyosiform erythroderma Congenital panfollicular nevus Congenital reticular ichthyosiform erythroderma Congenital smooth muscle hamartoma Cowden syndrome Crandall syndrome Cutaneous neuroendocrine carcinoma Cystic hygroma Deaf blind hypopigmentation syndrome, Yemenite type Dermatitis herpetiformis Dermatofibrosarcoma protuberans Dermatopathia pigmentosa reticularis Didymosis aplasticosebacea Diffuse cutaneous systemic sclerosis Diffuse lymphatic malformation Dowling-Degos disease Drug-induced lupus erythematosus Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria Dyskeratosis congenita Epidermal nevus syndrome Erdheim-Chester disease Erythrokeratodermia variabilis Exfoliative ichthyosis Extranodal nasal NK/T cell lymphoma Familial cylindromatosis Familial generalized lentiginosis Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Familial keratoacanthoma Familial melanoma Familial multiple fibrofolliculoma Familial multiple trichoepithelioma Familial normophosphatemic tumoral calcinosis Familial progressive hyper- and hypopigmentation Familial progressive hyperpigmentation Familial tumoral calcinosis Follicular atrophoderma-basal cell carcinoma Frontal fibrosing alopecia Frontonasal dysplasia with alopecia and genital anomaly Gardner syndrome Generalized basaloid follicular hamartoma syndrome Generalized eruptive histiocytosis Generalized peeling skin syndrome Generalized pustular psoriasis Gingival fibromatosis-hypertrichosis syndrome Gorlin syndrome Graham Little-Piccardi-Lassueur syndrome Granulomatous slack skin Griscelli disease Griscelli disease type 1 Griscelli disease type 2 Griscelli disease type 3 H syndrome Hair anomaly Hair defect-photosensitivity-intellectual disability syndrome Harlequin ichthyosis Hemihyperplasia-multiple lipomatosis syndrome Hereditary hypotrichosis with recurrent skin vesicles Hereditary leiomyomatosis and renal cell cancer Hereditary progressive mucinous histiocytosis Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome type 7 Hermansky-Pudlak syndrome type 8 Hermansky-Pudlak syndrome type 9 Hermansky-Pudlak syndrome with neutropenia Hermansky-Pudlak syndrome with pulmonary fibrosis Hermansky-Pudlak syndrome without pulmonary fibrosis Herpetiform pemphigus Hyperkeratosis-hyperpigmentation syndrome Hyperpigmentation of the skin Hypertrichosis Hypertrichosis cubiti Hypertrichosis lanuginosa congenita Hypertrichosis-acromegaloid facial appearance syndrome Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome Hypopigmentation of the skin Hypotrichosis simplex Hypotrichosis simplex of the scalp Hypotrichosis-deafness syndrome Ichthyosis Ichthyosis follicularis-alopecia-photophobia syndrome Ichthyosis hystrix gravior Ichthyosis hystrix of Curth-Macklin Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Ichthyosis-hypotrichosis syndrome Ichthyosis-oral and digital anomalies syndrome Ichthyosis-prematurity syndrome Indeterminate cell histiocytosis Indolent primary cutaneous B-cell lymphoma Indolent primary cutaneous T-cell lymphoma Infantile digital fibromatosis Infantile myofibromatosis Infantile onset panniculitis with uveitis and systemic granulomatosis Inflammatory linear verrucous epidermal nevus Inherited ichthyosis syndromic form Isolated anterior cervical hypertrichosis Isolated hair shaft abnormality Ito hypomelanosis Juvenile xanthogranuloma KID syndrome Kein Name gefunden Kein Name gefunden Keratinopathic ichthyosis Keratoderma hereditarium mutilans with ichthyosis Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Lamellar ichthyosis Large congenital melanocytic nevus Ledderhose disease Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Lichen planopilaris Limited cutaneous systemic sclerosis Limited systemic sclerosis Linear IgA dermatosis Linear and whorled nevoid hypermelanosis Linear nevus sebaceus syndrome Linear verrucous nevus syndrome Localized scleroderma Loose anagen syndrome MEDNIK syndrome Macrocystic lymphatic malformation Malignant melanoma of the mucosa Marie Unna hereditary hypotrichosis Microcystic lymphatic malformation Minimal pigment oculocutaneous albinism type 1 Monilethrix Mucous membrane pemphigoid Muir-Torre syndrome Multicentric reticulohistiocytosis Multiple self-healing squamous epithelioma Mycosis fungoides and variants NEVADA syndrome Naegeli-Franceschetti-Jadassohn syndrome Necrobiotic xanthogranuloma Netherton syndrome Neurocutaneous melanocytosis Nevus comedonicus syndrome Nevus of Ito Nevus of Ota Non-Langerhans cell histiocytosis Noonan syndrome-like disorder with loose anagen hair Oculocerebral hypopigmentation syndrome, Cross type Oculocutaneous albinism Oculocutaneous albinism type 1 Oculocutaneous albinism type 1A Oculocutaneous albinism type 1B Oculocutaneous albinism type 2 Oculocutaneous albinism type 3 Oculocutaneous albinism type 4 Oculocutaneous albinism type 5 Oculocutaneous albinism type 6 Oculocutaneous albinism type 7 Oley syndrome Onychocytic matricoma Onychomatricoma Osteopathia striata-pigmentary dermopathy-white forelock syndrome Osteosclerosis-ichthyosis-premature ovarian failure syndrome PENS syndrome PTEN hamartoma tumor syndrome Papular xanthoma Paraneoplastic pemphigus Peeling skin syndrome Peeling skin syndrome type A Peeling skin syndrome type B Peeling skin syndrome type C Pemphigoid gestationis Pemphigus erythematosus Pemphigus foliaceus Pemphigus vegetans Pemphigus vulgaris Phakomatosis cesioflammea Phakomatosis cesiomarmorata Phakomatosis pigmentokeratotica Phakomatosis pigmentovascularis Phakomatosis spilorosea Piebald trait-neurologic defects syndrome Piebaldism Pigmentation anomaly of the skin Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Pili bifurcati Pili gemini Pili torti Pili torti-developmental delay-neurological abnormalities syndrome 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 Progressive nodular histiocytosis Proliferating trichilemmal cyst Proteus syndrome Proteus-like syndrome Pseudopelade of Brocq Pyoderma gangrenosum-acne-suppurative hidradenitis syndrome Pyogenic arthritis-pyoderma gangrenosum-acne syndrome Quinquaud's folliculitis decalvans Rare lymphatic malformation Rare nail tumor Rare nevus Rare skin tumor or hamartoma Recessive X-linked ichthyosis Reticulate acropigmentation of Kitamura Reynolds syndrome Ringed hair disease Rombo syndrome SCALP syndrome Salt-and-pepper syndrome Scleroderma Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Self-improving collodion baby Sjögren-Larsson syndrome Subcutaneous panniculitis-like T-cell lymphoma Superficial epidermolytic ichthyosis Superficial fibromatosis Superficial pemphigus Syndromic hair shaft abnormality Syndromic oculocutaneous albinism Syndromic recessive X-linked ichthyosis Syringocystadenoma papilliferum Systemic disease with skin involvement Systemic sclerosis Sézary syndrome Temperature-sensitive oculocutaneous albinism type 1 Terminal osseous dysplasia-pigmentary defects syndrome Tietz syndrome Tricho-dento-osseous syndrome Trichodental syndrome Trichodysplasia-xeroderma syndrome Trichofolliculoma Trichothiodystrophy Tuberous sclerosis complex Uncombable hair syndrome Verrucous nevus Waardenburg syndrome Waardenburg syndrome type 1 Waardenburg syndrome type 2 Waardenburg syndrome type 3 White sponge nevus Woolly hair Woolly hair nevus Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome X-linked congenital generalized hypertrichosis X-linked dominant chondrodysplasia punctata Xanthoma disseminatum