Klinik und Poliklinik für Dermatologie, Venerologie und Allergologie am Universitätsklinikum Würzburg Assigned diseases:
In the following you will find the diseases that are treated in this facility:
ANE syndrome
Acanthokeratolytic verrucous nevus
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 cataract-ichthyosis syndrome
Congenital generalized hypertrichosis, Ambras type
Congenital ichthyosiform erythroderma
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome
Congenital ichthyosis-microcephalus-tetraplegia syndrome
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
Epidermolysis bullosa acquisita
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-alopecia-genital anomalies syndrome
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 syndrome
Griscelli syndrome type 1
Griscelli syndrome type 2
Griscelli syndrome 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 due to AP-3 deficiency
Hermansky-Pudlak syndrome due to BLOC-1 deficiency
Hermansky-Pudlak syndrome due to BLOC-2 deficiency
Hermansky-Pudlak syndrome due to BLOC-3 deficiency
Hermansky-Pudlak syndrome type 8
Hermansky-Pudlak syndrome type 9
Herpetiform pemphigus
Hyperkeratosis-hyperpigmentation syndrome
Hyperpigmentation of the skin
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-cheek-eyebrow 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
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
PAPA syndrome
PASH 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
Quinquaud folliculitis decalvans
Rare disorder with hypertrichosis
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