Deutsch
Clinical AreaChirurgie
Associated diseases
- [Pleuro]pulmonary blastoma
- Anorectal malformations, [non-]syndromic; differential diagnosis
- Aortectasia, thoracic [EBM 11448}
- Aortectasia, thoracic; differential diagnosis
- Breast cancer / therapy with PARP inhibitors
- Brustkrebs- und Eierstockkrebs, hereditär (HBOC)
- Choanal atresia, differential diagnosis
- Colon cancer, hereditary non-polyposis; differential diagnosis
- Colon carcinoma, POLD1-related
- Colorectal cancers, hereditary; differential diagnosis
- Cowden syndrome, differential diagnosis
- Currarino triad
- Cystische Fibrose, Differentialdiagnose
- Diaphragmatic hernias, congenital, differential diagnosis
- Ductal plate malformations, differential diagnosis
- Esophageal squamous cell cancer [susceptibility]
- Frontonasal dysplasia + Opitz GBBB syndrome, differential diagnosis
- Gastric cancer, hereditary diffuse; in part multifactorial; differential diagnosis
- Gastrointestinal tumors, monogeneic; differential diagnosis
- Gynaecological tumors based on familial predisposition for inherited cancers
- Head and neck cancer, susceptibility
- Hearing loss with (ear) malformations, differential diagnosis
- Inflammatory bowel diseases + infantile enterocolitis, monogenic; DD
- Jeune syndrome, differential diagnosis
- Kidney cysts, medullary, type 1+2
- Kolonkarzinom, POLE related
- Li-Fraumeni syndrome, differential diagnosis
- Lung cancer, SCLC; susceptibility + protection
- Lungenkarzinom, Adeno-Ca; Suszeptibilität + Protektion
- Medullary-cystic kidney disease [ADTKD], differential diagnosis
- Morbus Crohn, genetic predisposition
- Morbus Hirschsprung, familial; differential diagnosis
- Morbus Hirschsprung, syndromic; differential diagnosis
- Multiple endocrine neoplasia, MEN; differential diagnosis
- Multiple endocrine tumors, differential diagnosis
- Neurofibromatosis, NF1; differential diagnosis
- Omphalocele, laparoschisis; differential diagnosis
- Pancreatic cancer [susceptibility loci]
- Pankreas-Karzinom
- Pankreas-Karzinom - PARP-Inhibitor-Therapie
- Paraganglioma / pheochromocytoma, differential diagnosis
- Paraganglioma 1 / phaeochromocytoma
- Paraganglioma 3 / phaeochromocytoma
- Paraganglioma 4 / phaeochromocytoma
- Parathyroid cancer, differential diagnosis
- Pediatric tumor predisposition, hereditary
- Pendred syndrome, differential diagnosis
- Peritoneal carcinoma / PARP inhibitor therapy
- Peutz-Jeghers syndrome
- Poly-/syndactyly, pre- + postaxial; differential diagnosis
- Polycystic kidney disease, ADPKD; differential diagnosis
- Polycystic kidney disease, ARPKD; differential diagnosis
- Polycystic liver disease, differential diagnosis
- Polyposis coli, differential diagnosis
- Polyposis syndrome, juvenile
- Polyposis syndrome, serrated; differential diagnosis
- Polyposis, APC-assoiated, differential diagnosis
- Polyposis, familial adenomatous 3
- Polyposis, familial adenomatous 4
- Polyposis, familial adenomatous; FAP
- Renal disease, familial cystic; differential diagnosis
- Rhabdoid tumor predisposition
- Rhabdomyosarcoma, familial; differential diagnosis
- Short bowel syndrome, congenital
- Signet ring cell carcinoma, gastric; differential diagnosis
- Stomach cancer, predisposition
- Thyroid carcinoma, familial, non-medullary; differential diagnosis
- Thyroid carcinoma, hereditary medullary; differential diagnosis
- Thyroid carcinoma, hereditary; differential diagnosis
- Tricho-hepato-enteric syndrome, differential diagnosis
- Tumor progression (CNI-monitor for therapy control)
- von Hippel-Lindau syndrome
- Wilms tumor [including susceptibility], differential diagnosis
- WT1 disorder; DD congenital diaphragmatic hernia
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).