Deutsch
Clinical AreaDermatology
Associated diseases
- Adams-Oliver syndrome, differential diagnosis
- Aicardi-Goutières syndrome, differential diagnosis
- Akne inversa, familial; differential diagnosis
- Albinism, ocular/oculocutaneous; differential diagnosis
- Alkaptonuria, differential diagnosis
- Alopcia cicatricial, differential diagnosis
- Alopecia universalis
- Alopecia, syndromal; differential diagnosis
- Angioedema, hereditary
- Anonychia, differential diagnosis
- Ataxia telangiectasia
- Birt-Hogg-Dubé syndrome, differential diagnosis
- Bloom syndrome, differential diagnosis
- Brooke-Spiegler syndrome / CYLD cutaneous syndrome, differential diagnosis
- Cardio-facio-cutaneous syndrome, differential diagnosis
- Cartilage-hair hypoplasia / anauxetic dysplasia spectrum, differential diagnosis
- Chediak-Higashi syndrome
- CHILD / CK syndrome, differential diagnosis
- Cockayne syndrome
- Cockayne syndrome, differential diagnosis
- Cowden syndrome, differential diagnosis
- Cutis laxa, differential diagnosis
- Dermopathie, restriktive; Differentialdiagnose
- Dyskeratosis congenita, differential diagnosis
- Dyskeratosis congenita, X-chromosomal
- Ectodermal dysplasia, hypohydrotic; differential diagnosis
- Ehlers-Danlos syndrome, vascular type
- Ektodermale Dysplasie, hydrotische, Clouston; Differentialdiagnose
- Ektodermale Dysplasie, ohne An-/Hypohydrosis; Differentialdiagnose
- Epidermodysplasia verruciformis, differential diagnosis
- Epidermolysis bullosa dystrophica, differential diagnosis
- Epidermolysis bullosa simplex with pyloric atresia, differential diagnosis
- Epidermolysis bullosa simplex, differential diagnosis
- Epidermolysis bullosa, differential diagnosis
- Epidermolysis bullosa, junctional; differential diagnosis
- Erythromelalgia, primary
- FAMMM syndrome, differential diagnosis
- Genodermatoses with malignant degeneration, differential diagnosis
- Goltz[-Gorlin]-Syndrom, differential diagnosis
- Gorlin syndrome, differential diagnosis
- Hamartomas [extra-gastrointestinal], differential diagnosis
- Head and neck cancer, susceptibility
- Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome, differential diagnosis
- Hermansky-Pudlak syndrome, differential diagnosis
- Hyaline fibromatosis syndrome, differential diagnosis
- Hydroa vacciniforme
- Hypertrichosis, konnatal; Differentialdiagnose
- Ichthyoses, syndromic; differential diagnosis
- Ichthyosis + related dyskeratinoses, differential diagnosis
- Ichthyosis, congenital, recessive; differential diagnosis
- Immunodeficiency, primary; differential diagnosis
- Keratosis, keratoderma, erythrokeratoderma; differential diagnosis
- Kindler syndrome, differential diagnosis
- Legius syndrome; differential diagnosis
- Leiomyomatosis, + renal cell cancer; differential diagnosis
- Lipodystrophy, familial; differential diagnosis
- Lipoidproteinosis, differential diagnosis
- Lipomatosis, differential diagnosis
- Loeys-Dietz-/ Marfan-/ vaskuläres Ehlers-Danlos-Syndrom, Differentialdiagnose
- Lupus [erythematosus], "monogenic"; differential diagnosis
- Lupus erythematodes, susceptibility
- Mastocytosis, differential diagnosis
- Melanoma + renal carcinoma, MITF-associated
- Melanomas, familial + uveal; differential diagnosis
- Merkel cell carcinoma, early onset; predisposition
- Microcephaly-Capillary Malformation Syndrome, differential diagnosis
- Microphthalmia with Linear Skin Defects Syndrome, differential diagnosis
- Milroy disease, differential diagnosis
- Morbus Fabry
- Morbus Fabry, differential diagnosis
- Morbus Gaucher, DD congenital ichthyosis, AR
- Morbus Gaucher, differential diagnosis
- Morbus Schindler
- Mucocutaneous venous malformations; differential diagnosis
- Multiple benign monogenic skin tumors, differential diagnosis
- Myhre syndrome, differential diagnosis
- Naevus, epidermal; differential diagnosis
- Nail dysplasia, congenital; differential diagnosis
- Nail-patella syndrome
- Neurofibromatosis, NF1; differential diagnosis
- Osteopathia striata - cranial sclerosis, differential diagnosis
- Pachyonychia congenita, differential diagnosis
- Peeling-skin syndrome, differential diagnosis
- Peutz-Jeghers syndrome
- Pfeiffer syndrome 1-3
- Photosensitivity, cutaneous; differential diagnosis
- Piebaldism, differential diagnosis
- Polyposis coli, differential diagnosis
- Porokeratosis, familial; differential diagnosis
- Porphyria, differential diagnosis
- Porphyria, erythropoetic 1
- Pseudoxanthoma elasticum, differential diagnosis
- Psoriasis, generalised pustular; differential diagnosis
- PTEN hamartoma tumor syndrome
- Rendu-Osler-Weber disease, differential diagnosis
- Rickets, hypophosphataemic; differential diagnosis
- Sensenbrenner syndrome, differential diagnosis
- Stiff-skin syndrome, differential diagnosis
- Sulfatase deficiency, multiple
- Sulfatase deficiency, multiple; differential diagnosis
- Tuberous sclerosis, differential diagnosis
- Vascular skin disorders, differential diagnosis
- Vasculopathy, retinal, with cerebral Leukencephalopathy + systemic manifestations
- White sponge naevus
- Wiskott-Aldrich syndrome, differential diagnosis
- Woolly hair syndrome, isolated; differential diagnosis
- Xeroderma pigmentosum, Trichothiodystrophy/ Cockayne syndrome; differential diagnosis
Notes on the clinical area
Here you will find the disease-related gene panels available for the clinical area specified above.
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