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 Tumors are often affected by both genetic factors and environmental factors. With the continuous progress of science and technology, more and more cancer genes have been clear. Among them, hereditary tumor is a disease caused by specific gene mutations.

    Mygenostics works together with experts on clinical tumor to develop a gene detection kit associated with hereditary cancer, involving a variety of cancers (see table below). It is a gene capture scheme to detect specific tumor for the individual patient, combined with the new generation high-throughput sequencing technology and bioinformatics analysis, to know specific genes and risks of tumors. It will adopt appropriate prevention and intervention measures based on the test results, so that to provide the scientific level clinicians effective individual treatment plan and predict cancer risk.
Neuroinoma Bladder cancer Pleural lung tumor
Colorectal cancer Gastrointestinal stromal tumor Non small cell lung cancer
Desmoid tumor Parathyroid adenoma Exostoses Multiple 1
Hepatoblastoma Pituitary tumor Exostoses Multiple 2
Neurospoagioma Islet cell tumor Leiomyomatosis
Leukemia Carcinoid tumor Birt-Hogg-Dube system
Acute myeloid leukemia Endometrial cancer Trichodiscoma
Leukemia(FANCB;FANCD1) Non Hodgkin lymphoma Hepatic adenoma
lymphoma Neurofibromatosis type2 Hepatocellular carcinoma
Medulloblastoma Papillary thyroid carcinoma Oral squamous carcinoma
Squamous cell carcinoma of the skin Hamartoma Paraganglioma
Gastrointestinal polyps Prostatic carcinoma Jejunum hamartoma
Breast cancer Eye cacer Testicular cancer
Ovarian cancer Small cell lung cancer Renal cell carcinoma
Rhabdomyosarcoma Osteosarcoma Tuberoussclerosis
Ossifying fibroma of jaw Medullary thyroid carcinoma Thyroid adenoma
Gastric cancer Pheochromocytoma Hemangioma
Melanoma Myelodysplastic syndrome Renal mother cell tumor
Cylindroma Renal carcinoma Cutaneous basal cell carcinoma
Other nervous system tumors Other tumors