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CTGA Database Listing
Arab Genomic Studies
Records found: 2744 Sort by:
  • Hemochromatosis
    OMIM # 235200
    HLAH, Hemochromatosis, Hereditary, HH, HFE Gene, HFE
  • HFE Gene
    OMIM # 613609
    HFE
  • Breast Cancer
    OMIM # 114480
    Breast Cancer, Familial, Breast Cancer, Familial Male
  • Breast Cancer 1 Gene
    OMIM # 113705
    BRCA1,
  • Lynch Syndrome I
    OMIM # 120435
    Colorectal Cancer, Hereditary Nonpolyposis, Type 1, HNPCC1, Colon Cancer, Familial Nonpolyposis, Type 1, FCC1, COCA1, Lynch Syndrome II
  • Arthrogryposis, Distal, Type 2A
    OMIM # 193700
    DA2A, Freeman-Sheldon Syndrome, FSS, Whistling Face-Windmill Vane Hand Syndrome, Craniocarpotarsal Dystrophy, Craniocarpotarsal Dysplasia
  • Von Hippel-Lindau Syndrome
    OMIM # 193300
    Von Hippel-Lindau Syndrome, Modifiers of, VHL
  • Tooth Agenesis, Selective, 4
    OMIM # 150400
    STHAG4, Tooth Agenesis, Selective, 4 with or without Ectodermal Dysplasia, Lateral Incisors, Absence of, Lateral Incisors, Pegged or Missing , Succedaneous Teeth, Agenesis of
  • Schopf-Schulz-Passarge Syndrome
    OMIM # 224750
    SSPS, Keratosis Palmoplantaris with Cystic Eyelids, Hypodontia, and Hypotrichosis, Eccrine Tumors with Ectodermal Dysplasia
  • Anodontia of Permanent Dentition
    OMIM # 206780
    Teeth, Permanent, Absence of
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