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- Ablepharon macrostomy syndrome
- Adult syndrome
- Albinism oculocutaneous tyrosinase-negative
- Albinism totalis
- Albinoidism, oculocutaneous
- Antiphospholipid syndrome
- Atopic dermatitis (overview)
- Atrichia congenita with horny cysts
- Bannayan-riley-ruvalcaba syndrome
- Birt-hogg-dubé syndrome
- Chondrodysplasia calcificans congenita
- Chronic mucocutaneous candidiasis
- Cockayne syndrome
- Conjunctivitis allergica
- Cronkhite-canada syndrome
- Crouzon syndrome
- Cutis marmorata teleangiectatica congenita
- Dubowitz syndrome
- Dyskeratosis hereditary benign intraepithelial
- Dyskeratosis congenita
- Epidermolysis bullosa junctionalis with pyloric atresia
- Erythema multiforme, minus-type
- Erythrokeratodermia progressive, type burns
- Early syphilis
- Goldenhar syndrome
- Gonoblenorrhoea
- Gorlin-chaudhry-moss syndrome
- Granulomatosis with polyangiitis
- Hermansky-pudlak syndrome
- Herpes simplex corneae
- Ectodermal dysplasia, hidrotic, autosomal dominant
- Hiv infection
- Hutchinson sign ii
- Hydroa vacciniforme
- Hypercholesterolemia familial autosomal dominant
- Hypomelanosis ito
- Hypotrichosis congenita hereditaria marie unna
- Ichthyosis x-linked recessive
- Ichthyosis vulgaris
- Keratoconjunctivitis photoelectrica
- Keratosis lichenoides chronica
- Oculocutaneous tyrosinemia
- Collagenoses
- Leopard syndrome
- Lyme borreliosis
- Marfan syndrome
- Möbius syndrome
- Behçet's disease
- Fabry's disease
- Wilson's disease
- Nevus melanocytic (overview)
- Nevus of Ota
- Nail-patella syndrome
- Neurofibromatosis noonan syndrome
- Neurofibromatosis (overview)
- Onchocerciasis
- Pachyonychia congenita
- Paraproteinemic skin diseases
- Pemphigus vulgaris
- Polyarteritis nodosa systemic
- Recurrent polychondritis
- Caterpillar conjunctivitis
- Reactive arthritis
- Giant cell arteritis
- Rosacea
- Sarcoidosis of the skin
- Mould penning flintstone mims syndrome
- Mucous membrane melanoma
- Mucous membrane pemphigoid
- Sicca symptoms
- Sjögren-larsson syndrome
- Sjögren's syndrome
- Scleroderma systemic
- Sphingolipidoses
- Staphylococcal scalded skin syndrome
- Stevens-johnson syndrome
- Sturge weber syndrome
- Systemic juvenile idiopathic arthritis (Still syndrome)
- Toxic epidermal necrolysis
- Trichooculodermovertebral syndrome
- Cutaneous tuberculosis (overview)
- Tuberous sclerosis
- Turner syndrome
- Vasculitis with essential cryoglobulinemia
- Waardenburg syndrome (overview)
- Xanthogranuloma necrobiotic with paraproteinemia
- Xeroderma pigmentosum
- Zoster ophthalmicus
- Cytomegalovirus