Deutsch
Clinical AreaGeneral medicine
Associated diseases
- 46XY infertility / sterility
- Achromatopsia, differential diagnosis
- Adipositas, schwer, pur, früh; Differentialdiagnose
- Alkohol-Intoleranz, Differentialdiagnose
- Alopecia, syndromal; differential diagnosis
- Autoimmun-hämolytische Anämie; Differentialdiagnose
- Bewegungsstörungen, Beginn im Erwachsenenalter; DD
- C9orf72-FTD + C9orf72-ALS; erweiterte Differentialdiagnose
- Cancer precaution panel, genetic [private medical service]
- Cancer predisposition for solid tumors, adults
- Chromosomen-Aberration, postnatal
- Crigler-Najjar-Syndrom Typ I, unkonjugierte Hyperbilirubinämie
- Crigler-Najjar-Syndrom Typ II, unkonjugierte Hyperbilirubinämie
- Demenz, Manifestation<60 Jahre, familiäre Häufung oder frontotemporale Demenz
- Diabetes mellitus, genetisch bedingt; Differentialdiagnose
- Diabetes mellitus, type 2, susceptibility
- Dwarfism, idiopathic; differential diagnosis
- Epilepsie, erbliche Syndrome, Differentialdiagnose
- Familial mediterranean fever
- Fieber-Syndrome, hereditäre periodische; Differentialdiagnose
- Fragile-X syndrome
- Gilbert-[Meulengracht-]Syndrom, unkonjugierte Hyperbilirubinämie
- Gilbert-Syndrom, unkonjugierte Hyperbilirubinämie
- Glaukom, adultes Weitwinkel-; Suszeptibilität
- Hämaturie, familiäre, Differentialdiagnose
- Hörverlust, großes Panel inkl. Syndrome; Differentialdiagnose
- Hypercholesterolaemia, familial; differential diagnosis
- Hyperlipoproteinaemia, type III
- Hyperthyroidism; differential diagnosis
- Hypobeta-lipoproteinemia, differential diagnosis
- Hypomagnesiämie, genetisch bedingt; Differentialdiagnose
- Ichthyosen, syndromisch; Differentialdiagnose
- Ichthyosis + related dyskeratinoses, differential diagnosis
- Kleinwuchs, idiopathisch, familiär; SHOX-Gen
- Kleinwuchs, idiopatisch; SHOX-Gen
- Lipoprotein lipase deficiency, differential diagnosis
- Lippen-Kiefer-Gaumen-[Gesichts-]Spalten, Differentialdiagnose
- Lippen-Kiefer-Gaumen-[Gesichts-]Spalten, nicht-syndromal; Differentialdiagnose
- Mentale Retardierung - intellektuelle Defizite; Differentialdiagnose
- Mentale Retardierung bei [ponto-]zerebellärer Hypoplasie, Differentialdiagnose
- Morbus Bechterew
- Morbus Fabry
- Morbus Fabry, Differentialdiagnose
- MTHFR-Defizienz (RFLP)
- MTHFR-Defizienz (Sequenzierung)
- Mucocutaneous venous malformations; differential diagnosis
- Nail dysplasia, congenital; differential diagnosis
- Neutropenia, cyclic; differential diagnosis
- Neutropenie, kongenital; Differentialdiagnose
- Overgrowth syndromes, differential diagnosis
- PFAPA-Syndrom, Prädisposition/Assoziation; Differentialdiagnose
- Retinitis pigmentosa, syndromal; Differentialdiagnose
- Schlafstörungen, sekundär; Differentialdiagnose
- Schlaganfall, Differentialdiagnose
- Skeletal dysplasia, differential diagnosis
- Small stature, differential diagnosis
- Spermatogenese-Störungen, Differentialdiagnose
- Statin toxicity
- Teratozoospermie, Differentialdiagnose
- Trimethylaminuria, primary; differential diagnosis
- Tumor-Schnittmengen panel
- VEXAS-Syndrom
- Virus-Resistenz, Differentialdiagnose
Notes on the clinical area
Here you will find the disease-related gene panels available for the clinical area specified above.
If you cannot find the disease you are looking for, please use a known synonym in the search (also in English).