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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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