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)
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