Deutsch
Clinical AreaGeneral medicine
Associated diseases
- 46XY infertility / sterility, differential diagnosis
- Achromatopsia, differential diagnosis
- Adipositas, severe, pure, early onset; differential diagnosis
- Alcohol intolerance, differential diagnosis
- Alopecia, syndromal; differential diagnosis
- Autoimmune hemolytic anemia; differential diagnosis
- C9orf72-FTD + C9orf72-ALS; expanded differential diagnosis
- Cancer precaution panel, genetic [private medical service]
- Cancer predisposition for solid tumors, adults
- Chromosomen-Aberration, postnatal
- Clefting, differential diagnosis; differential diagnosis
- Clefting, non-syndromal; differential diagnosis
- Crigler-Najjar syndrome type I, unconjugated hyperbilirubinemia
- Crigler-Najjar syndrome type II, unconjugated hyperbilirubinemia
- Demenz, Manifestation<60 Jahre oder familiäre Häufung
- Diabetes mellitus, genetic; differential diagnosis
- Diabetes mellitus, type 2, susceptibility
- Dwarfism, idiopathic; differential diagnosis
- Epilepsy, inherited syndromes, differential diagnosis
- Familial mediterranean fever
- Fever syndromes, hereditary periodic; differential diagnosis
- Fragile-X syndrome
- Frontotemporal dementia (C9orf72) - Amyotrophic Lateralsklerosis; differential diagnosis
- Gilbert [Meulengracht] syndrome, unconjugated hyperbilirubinemia
- Gilbert syndrome, unconjugated hyperbilirubinemia
- 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
- Hypomagnesaemia, hereditary; differential diagnosis
- Ichthyoses, syndromic; differential diagnosis
- Ichthyosis + related dyskeratinoses, differential diagnosis
- Intellectual deficit - mental retardation, differential diagnosis
- Intellectual deficit + [ponto-]cerebellar hypoplasia, differential diagnosis
- Kleinwuchs, idiopathisch, familiär; SHOX-Gen
- Kleinwuchs, idiopatisch; SHOX-Gen
- Lipoprotein lipase deficiency, differential diagnosis
- Morbus Bechterew
- Morbus Fabry
- Morbus Fabry, differential diagnosis
- Movement disorders, adult onset; differential diagnosis
- MTHFR-Defizienz (RFLP)
- MTHFR-Defizienz (Sequenzierung)
- Mucocutaneous venous malformations; differential diagnosis
- Nail dysplasia, congenital; differential diagnosis
- Neutropenia, congenital; differential diagnosis
- Neutropenia, cyclic; differential diagnosis
- Overgrowth syndromes, differential diagnosis
- PFAPA syndrome, predisposition/association; differential diagnosis
- Resistance to viral infections, differential diagnosis
- Retinitis pigmentosa, syndromal; differential diagnosis
- Skeletal dysplasia, differential diagnosis
- Sleep disorders, secondary; differential diagnosis
- Small stature, differential diagnosis
- Spermatogenesis, disturbed; differential diagnosis
- Statin toxicity
- Stroke, differential diagnosis
- Teratozoospermia, differential diagnosis
- Trimethylaminuria, primary; differential diagnosis
- Tumour intersecting set panel
- VEXAS-Syndrom
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).