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OMIN数据库里面跟cancer相关的条目

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发表于 2017-3-2 15:09:37 | 显示全部楼层 |阅读模式
其实应该自己去看omin数据库:
MIM Number        Title
OMIM:109400        BASAL CELL NEVUS SYNDROME; BCNS
OMIM:109800        BLADDER CANCER
OMIM:114480        BREAST CANCER
OMIM:114500        COLORECTAL CANCER; CRC
OMIM:114550        HEPATOCELLULAR CARCINOMA
OMIM:120435        LYNCH SYNDROME I
OMIM:133239        ESOPHAGEAL CANCER
OMIM:137215        GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC
OMIM:144700        RENAL CELL CARCINOMA, NONPAPILLARY; RCC
OMIM:148500        TYLOSIS WITH ESOPHAGEAL CANCER; TOC
OMIM:150800        HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC
OMIM:155240        THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC
OMIM:158320        MUIR-TORRE SYNDROME; MRTES
OMIM:167000        OVARIAN CANCER
OMIM:171400        MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA; MEN2A
OMIM:176807        PROSTATE CANCER
OMIM:188470        THYROID CARCINOMA, FOLLICULAR; FTC
OMIM:188550        THYROID CARCINOMA, PAPILLARY
OMIM:191600        URETER, CANCER OF
OMIM:202300        ADRENOCORTICAL CARCINOMA, HEREDITARY; ADCC
OMIM:211980        LUNG CANCER
OMIM:246470        LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER
OMIM:260350        PANCREATIC CANCER
OMIM:260500        PAPILLOMA OF CHOROID PLEXUS; CPP
OMIM:273300        TESTICULAR GERM CELL TUMOR; TGCT
OMIM:275355        SQUAMOUS CELL CARCINOMA, HEAD AND NECK; HNSCC
OMIM:276300        MISMATCH REPAIR CANCER SYNDROME; MMRCS
OMIM:300854        RENAL CELL CARCINOMA, Xp11-ASSOCIATED; RCCX1
OMIM:312300        ANDROGEN INSENSITIVITY, PARTIAL; PAIS
OMIM:601228        POLYPOSIS SYNDROME, HEREDITARY MIXED, 1; HMPS1
OMIM:601518        PROSTATE CANCER, HEREDITARY, 1; HPC1
OMIM:603641        NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA
OMIM:603688        PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY
OMIM:603956        CERVICAL CANCER
OMIM:604370        BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1
OMIM:605074        RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1
OMIM:606719        MELANOMA-PANCREATIC CANCER SYNDROME
OMIM:608089        ENDOMETRIAL CANCER
OMIM:608266        PARATHYROID CARCINOMA
OMIM:608615        OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS
OMIM:609310        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2
OMIM:610644        PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL
OMIM:612229        COLORECTAL CANCER, SUSCEPTIBILITY TO, 3; CRCS3
OMIM:612555        BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2
OMIM:612591        COLORECTAL CANCER, SUSCEPTIBILITY TO, 10; CRCS10
OMIM:613244        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8; HNPCC8
OMIM:613347        PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
OMIM:613659        GASTRIC CANCER
OMIM:614331        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6
OMIM:614337        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4; HNPCC4
OMIM:614350        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5; HNPCC5
OMIM:614385        COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7; HNPCC7
OMIM:614456        MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8; CMM8
OMIM:614564        CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS
OMIM:615083        COLORECTAL CANCER, SUSCEPTIBILITY TO, 12; CRCS12



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