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 ABDOMINAL AORTIC ANEURYSM(OMIM機械翻訳
 ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL(OMIM機械翻訳
 ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER(OMIM機械翻訳
 ACHARD SYNDROME(OMIM機械翻訳
 ACHONDROPLASIA; ACH(OMIM機械翻訳
 NEUROFIBROMATOSIS, TYPE II; NF2(OMIM機械翻訳
 APERT SYNDROME(OMIM機械翻訳
 ACROFACIAL DYSOSTOSIS, CATANIA TYPE(OMIM機械翻訳
 ACROKERATOELASTOIDOSIS; AKE(OMIM機械翻訳
 ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA(OMIM機械翻訳
 ACROMEGALOID FACIAL APPEARANCE SYNDROME(OMIM機械翻訳
 ACROMICRIC DYSPLASIA(OMIM機械翻訳
 ADULT SYNDROME(OMIM機械翻訳
 AGLOSSIA-ADACTYLIA(OMIM機械翻訳
 TIETZ SYNDROME(OMIM機械翻訳
 ALOPECIA AREATA(OMIM機械翻訳
 ALOPECIA CONGENITA WITH KERATOSIS PALMOPLANTARIS(OMIM機械翻訳
 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY(OMIM機械翻訳
 ALPHA-GALACTOSIDASE B; GALB(OMIM機械翻訳
 ALZHEIMER DISEASE; AD(OMIM機械翻訳
 AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE(OMIM機械翻訳
 AMELOONYCHOHYPOHIDROTIC SYNDROME(OMIM機械翻訳
 ANAPLASTIC LYMPHOMA KINASE; ALK(OMIM機械翻訳
 ANEURYSM, INTRACRANIAL BERRY(OMIM機械翻訳
 ANGELMAN SYNDROME; AS(OMIM機械翻訳
 ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA; ASPED(OMIM機械翻訳
 ANGIOEDEMA, HEREDITARY; HAE(OMIM機械翻訳
 ANIRIDIA; AN1(OMIM機械翻訳
 ANIRIDIA AND ABSENT PATELLA(OMIM機械翻訳
 ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE(OMIM機械翻訳
 ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE(OMIM機械翻訳
 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES(OMIM機械翻訳
 TOWNES-BROCKS SYNDROME; TBS(OMIM機械翻訳
 APLASIA CUTIS CONGENITA(OMIM機械翻訳
 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1(OMIM機械翻訳
 ARTHROGRYPOSIS MULTIPLEX CONGENITA; AMC(OMIM機械翻訳
 ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 1; AMCD1(OMIM機械翻訳
 ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II(OMIM機械翻訳
 ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE II, WITH CRANIOFACIAL ABNORMALITIES(OMIM機械翻訳
 ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES(OMIM機械翻訳
 STICKLER SYNDROME, TYPE I; STL1(OMIM機械翻訳
 N-ACETYLTRANSFERASE 1; NAT1(OMIM機械翻訳
 AUROCEPHALOSYNDACTYLY(OMIM機械翻訳
 AUTOIMMUNE DISEASES(OMIM機械翻訳
 AXIAL OSTEOMALACIA(OMIM機械翻訳
 MACHADO-JOSEPH DISEASE; MJD(OMIM機械翻訳
 BASAL CELL NEVUS SYNDROME; BCNS(OMIM機械翻訳
 BEHCET SYNDROME(OMIM機械翻訳
 BILIARY CIRRHOSIS, PRIMARY; PBC(OMIM機械翻訳
 BLADDER CANCER(OMIM機械翻訳
 BLUE RUBBER BLEB NEVUS(OMIM機械翻訳
 BOWING OF LEGS, ANTERIOR, WITH DWARFISM(OMIM機械翻訳
 BRACHYDACTYLY, COMBINED B AND E TYPES(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A1; BDA1(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A2; BDA2(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A3; BDA3(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A4; BDA4(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A5, WITH NAIL DYSPLASIA(OMIM機械翻訳
 BRACHYDACTYLY, TYPE A6; BDA6(OMIM機械翻訳
 BRACHYDACTYLY, TYPE C; BDC(OMIM機械翻訳
 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME(OMIM機械翻訳
 BRACHYMESOMELIA-RENAL SYNDROME(OMIM機械翻訳
 BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME(OMIM機械翻訳
 BURKITT LYMPHOMA; BL(OMIM機械翻訳
 CAFFEY DISEASE(OMIM機械翻訳
 CAFE-AU-LAIT SPOTS, MULTIPLE(OMIM機械翻訳
 CAMPTOBRACHYDACTYLY(OMIM機械翻訳
 CAMPTODACTYLY(OMIM機械翻訳
 HEPATOCELLULAR CARCINOMA(OMIM機械翻訳
 CARDIOFACIOCUTANEOUS SYNDROME(OMIM機械翻訳
 CAT EYE SYNDROME; CES(OMIM機械翻訳
 CATALASE; CAT(OMIM機械翻訳
 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION(OMIM機械翻訳
 CATARACT, CONGENITAL, VOLKMANN TYPE; CCV(OMIM機械翻訳
 CATARACT-MICROCORNEA SYNDROME(OMIM機械翻訳
 CENTRAL CORE DISEASE OF MUSCLE(OMIM機械翻訳
 CERVICAL VERTEBRAL FUSION, AUTOSOMAL DOMINANT(OMIM機械翻訳
 CHARCOT-MARIE-TOOTH DISEASE, TYPE 1B; CMT1B(OMIM機械翻訳
 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM(OMIM機械翻訳
 CHEILITIS GLANDULARIS(OMIM機械翻訳
 CHERUBISM(OMIM機械翻訳
 ALAGILLE SYNDROME; AGS(OMIM機械翻訳
 CLEFT HAND AND ABSENT TIBIA(OMIM機械翻訳
 VAN DER WOUDE SYNDROME; VWS(OMIM機械翻訳
 CLEIDORHIZOMELIC SYNDROME(OMIM機械翻訳
 CLUBFOOT(OMIM機械翻訳
 RENAL-COLOBOMA SYNDROME(OMIM機械翻訳
 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY(OMIM機械翻訳
 COLOBOMA OF OPTIC NERVE(OMIM機械翻訳
 COMPLEMENT COMPONENT 5 DEFICIENCY(OMIM機械翻訳
 CORNEODERMATOOSSEOUS SYNDROME(OMIM機械翻訳
 COSTOCORACOID LIGAMENT, CONGENITALLY SHORT(OMIM機械翻訳
 CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS(OMIM機械翻訳
 JACKSON-WEISS SYNDROME; JWS(OMIM機械翻訳
 CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS(OMIM機械翻訳
 CUTIS LAXA(OMIM機械翻訳
 DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY(OMIM機械翻訳
 DARIER-WHITE DISEASE; DAR(OMIM機械翻訳
 DEAFNESS AND ONYCHODYSTROPHY, DOMINANT FORM(OMIM機械翻訳
 DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OF FINGERS AND TOES(OMIM機械翻訳


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