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CTGA Database Listing
Arab Genomic Studies
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  • Beckwith-Wiedemann Syndrome
    OMIM # 130650
    BWS, EMG Syndrome, Exomphalos-Macroglossia-Gigantism Syndrome, Wiedemann-Beckwith Syndrome, WBS, Beckwith-Wiedemann Syndrome Chromosome Region, BWCR
  • Ehlers-Danlos syndrome, spondylodysplastic type, 1
    OMIM # 130070
    EDSSPD1, Ehlers-Danlos syndrome with short stature and limb anomalies, EDSSLA, Proteodermatan Sulfate, Defective Biosynthesis of, PDS, Defective Biosynthesis of, Dermatan Sulfate Proteoglycan, Xylosylprotein 4-Beta-Galactosyltransferase Deficiency, XGPT Deficiency, Galactosyltransferase I Deficiency
  • Ehlers-Danlos Syndrome, Hypermobility Type
    OMIM # 130020
    EDSHMB, Ehlers-Danlos Syndrome, Type III, EDS III, EDS3, Benign Hypermobility Syndrome
  • Ehlers-Danlos Syndrome, classic type, 1
    OMIM # 130000
    EDSCL1, Ehlers-Danlos Syndrome, type 1, Ehlers-Danlos Syndrome, Severe Classic Type, EDS I, EDS1, Ehlers-Danlos Syndrome, Gravis Type
  • Dysplasia Epiphysealis Hemimelica with Chondromas and Osteochondromas
    OMIM # 127820
    Osteochondromatosis, Dominant Carpotarsal, Dominant Carpotarsal Osteochondromatosis, DCO
  • Dyslexia, Susceptibility to, 1
    OMIM # 127700
    DYX1, Word-Blindness, Congenital, Reading Disability, Specific, 1, Dyslexia, Susceptibility to, 4, DYX4, Dyslexia, Susceptibility to, 7, DYX7
  • Leri-Weill Dyschondrosteosis
    OMIM # 127300
    LWD, Dyschondrosteosis, DCO, Madelung Deformity
  • Duane Retraction Syndrome 1
    OMIM # 126800
    DURS1, DRS, Duane Syndrome, DUS, Duane Anomaly, Retraction Syndrome
  • Multiple Sclerosis
    OMIM # 126200
    Disseminated Sclerosis, Multiple Sclerosis susceptibility 1, MS1, MS
  • Robinow Syndrome, Autosomal Recessive
    OMIM # 268310
    RRS, Costovertebral Segmentation Defect with Mesomelia, Covesdem Syndrome
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