GeneticSupportトップページへ もどる


 WEAVER SYNDROME(OMIM機械翻訳
 WEILL-MARCHESANI SYNDROME(OMIM機械翻訳
 WEISSENBACHER-ZWEYMULLER SYNDROME; WZS(OMIM機械翻訳
 WERNICKE-KORSAKOFF SYNDROME(OMIM機械翻訳
 WILSON DISEASE(OMIM機械翻訳
 WINCHESTER DISEASE(OMIM機械翻訳
 WOLFF MENTAL RETARDATION SYNDROME(OMIM機械翻訳
 WOLMAN DISEASE(OMIM機械翻訳
 WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS(OMIM機械翻訳
 WRINKLY SKIN SYNDROME; WSS(OMIM機械翻訳
 DE SANCTIS-CACCHIONE SYNDROME(OMIM機械翻訳
 XX MALE SYNDROME(OMIM機械翻訳
 YOUNG SYNDROME(OMIM機械翻訳
 ZUNICH NEUROECTODERMAL SYNDROME(OMIM機械翻訳
 DENT DISEASE(OMIM機械翻訳
 INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED(OMIM機械翻訳
 HETEROTOPIA, PERIVENTRICULAR(OMIM機械翻訳
 MENTAL RETARDATION, X-LINKED 14; MRX14(OMIM機械翻訳
 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM(OMIM機械翻訳
 LISSENCEPHALY, X-LINKED(OMIM機械翻訳
 ANDROGEN INSENSITIVITY SYNDROME; AIS(OMIM機械翻訳
 FETAL AKINESIA SYNDROME, X-LINKED(OMIM機械翻訳
 IMMUNONEUROLOGIC DISORDER, X-LINKED(OMIM機械翻訳
 ADRENOLEUKODYSTROPHY; ALD(OMIM機械翻訳
 COATS DISEASE(OMIM機械翻訳
 POLYMICROGYRIA, BILATERAL PERISYLVIAN(OMIM機械翻訳
 SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED; SCIDX1(OMIM機械翻訳
 ALBINISM, OCULAR, TYPE I; OA1(OMIM機械翻訳
 ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS; OASD(OMIM機械翻訳
 ALBINISM-DEAFNESS SYNDROME; ADFN(OMIM機械翻訳
 WISKOTT-ALDRICH SYNDROME; WAS(OMIM機械翻訳
 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE; AIH(OMIM機械翻訳
 ANEMIA, SIDEROBLASTIC, X-LINKED(OMIM機械翻訳
 ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT(OMIM機械翻訳
 ANENCEPHALY--SPINA BIFIDA(OMIM機械翻訳
 FABRY DISEASE(OMIM機械翻訳
 ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED(OMIM機械翻訳
 BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS(OMIM機械翻訳
 BRANCHIAL ARCH SYNDROME, X-LINKED(OMIM機械翻訳
 CALVARIAL HYPEROSTOSIS(OMIM機械翻訳
 CATARACT, CONGENITAL, WITH MICROCORNEA OR SLIGHT MICROPHTHALMIA(OMIM機械翻訳
 CATARACT-DENTAL SYNDROME(OMIM機械翻訳
 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1(OMIM機械翻訳
 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA(OMIM機械翻訳
 CHARGE-LIKE SYNDROME, X-LINKED(OMIM機械翻訳
 CHONDRODYSPLASIA PUNCTATA, BRACHYTELEPHALANGIC(OMIM機械翻訳
 CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE; CDPX1(OMIM機械翻訳
 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2(OMIM機械翻訳
 CHOROIDEREMIA WITH DEAFNESS AND OBESITY(OMIM機械翻訳
 COLORBLINDNESS, BLUE-MONO-CONE-MONOCHROMATIC TYPE; CBBM(OMIM機械翻訳
 CORPUS CALLOSUM, AGENESIS OF, WITH CHORIORETINAL ABNORMALITY(OMIM機械翻訳
 CORPUS CALLOSUM, PARTIAL AGENESIS OF(OMIM機械翻訳
 CUTIS LAXA, X-LINKED(OMIM機械翻訳
 CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION(OMIM機械翻訳
 DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE, AND SEIZURES(OMIM機械翻訳
 DEAFNESS, CONDUCTIVE, WITH STAPES FIXATION(OMIM機械翻訳
 MOHR-TRANEBJAERG SYNDROME; MTS(OMIM機械翻訳
 DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED(OMIM機械翻訳
 EHLERS-DANLOS SYNDROME, TYPE V(OMIM機械翻訳
 FACIOGENITAL DYSPLASIA(OMIM機械翻訳
 FG SYNDROME; FGS1(OMIM機械翻訳
 GRANULOMAS, CONGENITAL CEREBRAL(OMIM機械翻訳
 HEMOPHILIA A(OMIM機械翻訳
 HEMOPHILIA B; HEMB(OMIM機械翻訳
 HETEROTAXY, VISCERAL, X-LINKED(OMIM機械翻訳
 HYPERGLYCEROLEMIA(OMIM機械翻訳
 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2(OMIM機械翻訳
 HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED(OMIM機械翻訳
 HYPOPHOSPHATEMIA, X-LINKED(OMIM機械翻訳
 HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1(OMIM機械翻訳
 ICHTHYOSIS, X-LINKED(OMIM機械翻訳
 ICHTHYOSIS AND MALE HYPOGONADISM(OMIM機械翻訳
 INCONTINENTIA PIGMENTI; IP(OMIM機械翻訳
 KALLMANN SYNDROME 1; KAL1(OMIM機械翻訳
 KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA(OMIM機械翻訳
 KERATOSIS FOLLICULARIS SPINULOSA DECALVANS CUM OPHIASI; KFSD(OMIM機械翻訳
 KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY(OMIM機械翻訳
 LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY(OMIM機械翻訳
 LOWE OCULOCEREBRORENAL SYNDROME; OCRL(OMIM機械翻訳
 SUTHERLAND-HAAN X-LINKED MENTAL RETARDATION SYNDROME; SHS(OMIM機械翻訳
 MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 1; MRX1(OMIM機械翻訳
 FRAGILE SITE, FOLIC ACID TYPE, RARE, FRA(X)(q28); FRAXE(OMIM機械翻訳
 MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS(OMIM機械翻訳
 WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS(OMIM機械翻訳
 MENTAL RETARDATION, X-LINKED, WITH GROWTH RETARDATION, DEAFNESS, AND MICROGENITALISM(OMIM機械翻訳
 MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA(OMIM機械翻訳
 METAPHYSEAL ANADYSPLASIA(OMIM機械翻訳
 MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS(OMIM機械翻訳
 MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD(OMIM機械翻訳
 EMERY-DREIFUSS MUSCULAR DYSTROPHY; EDMD(OMIM機械翻訳
 N SYNDROME; NSX(OMIM機械翻訳
 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1; CSNB1(OMIM機械翻訳
 NORRIE DISEASE; NDP(OMIM機械翻訳
 OPTICOACOUSTIC NERVE ATROPHY WITH DEMENTIA(OMIM機械翻訳
 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC(OMIM機械翻訳
 OSTEOPATHIA STRIATA WITH PIGMENTARY DERMOPATHY INCLUDING WHITE FORELOCK(OMIM機械翻訳
 OTOPALATODIGITAL SYNDROME(OMIM機械翻訳
 RETINITIS PIGMENTOSA 2; RP2(OMIM機械翻訳
 RETINOSCHISIS 1, X-LINKED, JUVENILE; RS1(OMIM機械翻訳
 RETT SYNDROME; RTT(OMIM機械翻訳


Copyright 2003 GeneticSupport. All Rights Reserved.
GeneticSupport


SEO [PR] 爆速!無料ブログ 無料ホームページ開設 無料ライブ放送