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 TYLOSIS WITH ESOPHAGEAL CANCER; TOC(OMIM機械翻訳
 KERATOSIS PALMOPLANTARIS PAPULOSA(OMIM機械翻訳
 KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL(OMIM機械翻訳
 KLEEBLATTSCHAEDEL SYNDROME(OMIM機械翻訳
 KLEIN-WAARDENBURG SYNDROME(OMIM機械翻訳
 KLEINE-LEVIN HIBERNATION SYNDROME(OMIM機械翻訳
 KLIPPEL-FEIL DEFORMITY, CONDUCTIVE DEAFNESS, AND ABSENT VAGINA(OMIM機械翻訳
 KLIPPEL-FEIL SYNDROME(OMIM機械翻訳
 KLIPPEL-TRENAUNAY-WEBER SYNDROME(OMIM機械翻訳
 KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS(OMIM機械翻訳
 KOK DISEASE(OMIM機械翻訳
 LACRIMOAURICULODENTODIGITAL SYNDROME; LADD(OMIM機械翻訳
 LANGER-GIEDION SYNDROME; LGS(OMIM機械翻訳
 LARYNGEAL ABDUCTOR PARALYSIS(OMIM機械翻訳
 LEGG-CALVE-PERTHES DISEASE(OMIM機械翻訳
 LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM(OMIM機械翻訳
 LERI PLEONOSTEOSIS(OMIM機械翻訳
 LIPODYSTROPHY, FAMILIAL PARTIAL; FPLD(OMIM機械翻訳
 LIPODYSTROPHY, PARTIAL, WITH RIEGER ANOMALY, SHORT STATURE, AND INSULINOPENIC DIABETES MELLITUS(OMIM機械翻訳
 LIPOMATOSIS, FAMILIAL BENIGN CERVICAL(OMIM機械翻訳
 LYMPHEDEMA, HEREDITARY I(OMIM機械翻訳
 MACROCEPHALY, BENIGN FAMILIAL(OMIM機械翻訳
 MACROGLOBULINEMIA, WALDENSTROM; WM(OMIM機械翻訳
 MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 2; MHS2(OMIM機械翻訳
 MALIGNANT HYPERTHERMIA SUSCEPTIBILITY 3(OMIM機械翻訳
 ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1(OMIM機械翻訳
 MARCUS GUNN PHENOMENON(OMIM機械翻訳
 MARFAN SYNDROME; MFS(OMIM機械翻訳
 MARSHALL SYNDROME(OMIM機械翻訳
 CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA(OMIM機械翻訳
 MEDULLARY THYROID CARCINOMA, FAMILIAL; MTC(OMIM機械翻訳
 MEDULLOBLASTOMA(OMIM機械翻訳
 MEGADUODENUM AND/OR MEGACYSTIS(OMIM機械翻訳
 MEGALODACTYLY(OMIM機械翻訳
 MELANOMA-ASTROCYTOMA SYNDROME(OMIM機械翻訳
 MENINGIOMA 1; MN1(OMIM機械翻訳
 MESOMELIC DYSPLASIA, KANTAPUTRA TYPE(OMIM機械翻訳
 METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE(OMIM機械翻訳
 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS(OMIM機械翻訳
 KNIEST DYSPLASIA(OMIM機械翻訳
 5-@METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE; MTR(OMIM機械翻訳
 MICROCEPHALY, AUTOSOMAL DOMINANT(OMIM機械翻訳
 MICHELIN TIRE BABY SYNDROME(OMIM機械翻訳
 MICROCEPHALY-DEAFNESS SYNDROME(OMIM機械翻訳
 MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL(OMIM機械翻訳
 MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA(OMIM機械翻訳
 MITRAL VALVE PROLAPSE, FAMILIAL; MVP(OMIM機械翻訳
 MOEBIUS SYNDROME 1; MBS1(OMIM機械翻訳
 MOLAR I REINCLUSION(OMIM機械翻訳
 MOMO SYNDROME(OMIM機械翻訳
 MUCOEPITHELIAL DYSPLASIA, HEREDITARY(OMIM機械翻訳
 MUIR-TORRE SYNDROME; MTS(OMIM機械翻訳
 MULLERIAN APLASIA(OMIM機械翻訳
 COWDEN DISEASE; CD(OMIM機械翻訳
 MUSCULAR ATROPHY, ADULT SPINAL(OMIM機械翻訳
 MYOCLONUS AND ATAXIA(OMIM機械翻訳
 MYOCLONUS, HEREDITARY, WITH PROGRESSIVE DISTAL MUSCULAR ATROPHY(OMIM機械翻訳
 MYOSITIS(OMIM機械翻訳
 DYSTROPHIA MYOTONICA 1(OMIM機械翻訳
 CARNEY COMPLEX, TYPE 1; CNC1(OMIM機械翻訳
 NAEGELI SYNDROME(OMIM機械翻訳
 NAIL-PATELLA SYNDROME; NPS(OMIM機械翻訳
 NARCOLEPSY(OMIM機械翻訳
 NASOPHARYNGEAL CARCINOMA(OMIM機械翻訳
 NAVICULAR BONE, ACCESSORY(OMIM機械翻訳
 NEMALINE MYOPATHY 1, AUTOSOMAL DOMINANT; NEM1(OMIM機械翻訳
 IgA NEPHROPATHY(OMIM機械翻訳
 NEPHROPATHY, FAMILIAL, WITH GOUT(OMIM機械翻訳
 NEURITIS WITH BRACHIAL PREDILECTION; NAPB(OMIM機械翻訳
 NEUROFIBROMATOSIS, TYPE I; NF1(OMIM機械翻訳
 NEUROFIBROMATOSIS, FAMILIAL INTESTINAL; NF3B(OMIM機械翻訳
 NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL; NF3A(OMIM機械翻訳
 NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI; NF4(OMIM機械翻訳
 NEUROPATHY, HEREDITARY SENSORY, TYPE I; HSN1(OMIM機械翻訳
 NEUTROPENIA, CHRONIC FAMILIAL(OMIM機械翻訳
 CYCLIC HEMATOPOIESIS(OMIM機械翻訳
 NEVI FLAMMEI, FAMILIAL MULTIPLE(OMIM機械翻訳
 NEVUS SEBACEUS OF JADASSOHN(OMIM機械翻訳
 NIEVERGELT SYNDROME(OMIM機械翻訳
 NOONAN SYNDROME 1; NS1(OMIM機械翻訳
 NOONAN-LIKE/MULTIPLE GIANT CELL LESION SYNDROME(OMIM機械翻訳
 OCULODIGITOESOPHAGODUODENAL SYNDROME(OMIM機械翻訳
 ODONTOMA-DYSPHAGIA SYNDROME(OMIM機械翻訳
 OMODYSPLASIA(OMIM機械翻訳
 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY(OMIM機械翻訳
 OPTIC NERVE HYPOPLASIA, FAMILIAL BILATERAL(OMIM機械翻訳
 OSLAM SYNDROME(OMIM機械翻訳
 OSSICULAR MALFORMATIONS, FAMILIAL(OMIM機械翻訳
 OSTEOMESOPYKNOSIS(OMIM機械翻訳
 OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS; OSCS(OMIM機械翻訳
 OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II(OMIM機械翻訳
 PACHYDERMOPERIOSTOSIS; PDP(OMIM機械翻訳
 PACHYONYCHIA CONGENITA, TYPE 1; PC1(OMIM機械翻訳
 PACHYONYCHIA CONGENITA, TYPE 2; PC2(OMIM機械翻訳
 PACMAN DYSPLASIA(OMIM機械翻訳
 PAGET DISEASE OF BONE 1; PDB1(OMIM機械翻訳
 PAGET DISEASE, EXTRAMAMMARY(OMIM機械翻訳
 PALPEBRAL COLOBOMA-LIPOMA SYNDROME(OMIM機械翻訳
 PANCREAS, ANNULAR(OMIM機械翻訳
 PANCREATITIS, HEREDITARY; PCTT(OMIM機械翻訳


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