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CTGA Database Listing
Arab Genomic Studies
Records found: 2310 Sort by:
  • Diabetes Mellitus, Permanent Neonatal
    OMIM # 606176
    PNDM, Diabetes Mellitus, Permanent, of Infancy, PDMI, Diabetes Mellitus, Permanent Neonatal, with Neurologic Features, Developmental Delay, Epilepsy, and Neonatal Diabetes, DEND
  • Eukaryotic Translation Initiation Factor 2-Alpha Kinase 3
    OMIM # 604032
    EIF2AK3 , Pancreatic EIF2-Alpha Kinase, PEK, PERK, Heme-Regulated EIF2-Alpha Kinase, HRI
  • ATP-Binding Cassette, Subfamily C, Member 8
    OMIM # 600509
    ABCC8, Sulfonylurea Receptor, SUR, SUR1, Sulfonylurea Receptor, Beta-Cell High-Affinity,
  • Potassium Channel, Inwardly Rectifying Subfamily J, Member 11
    OMIM # 600937
    KCNJ11, Potassium Channel, Inwardly Rectifying, BIR Subunit, Beta-Cell Inward Rectifier Subunit, BIR, Inwardly Rectifying Potassium Channel Kir6.2
  • Ichthyosiform Erythroderma, Congenital, Nonbullous, 1
    OMIM # 242100
    NCIE1, IECN1, Ichthyosiform Erythroderma, BROCQ Congenital, Nonbullous Form, Nonbullous Congenital Ichthyosiform Erythroderma 1, NCIE, CIE,
  • Ichthyosis Congenita, Harlequin Fetus Type
    OMIM # 242500
    Harlequin Ichthyosis, HI, 'Harlequin Fetus', Ichthyosis Fetalis
  • ATP-Binding Cassette, Subfamily A, Member 12
    OMIM # 607800
    ABCA12, ATP-Binding Cassette Transporter 12, ATP-Binding Cassette 12,
  • Ichthyosis, Lamellar, 1
    OMIM # 242300
    LI1, Ichthyosis Congenita, Lamellar Exfoliation of Newborn, Desquamation of Newborn, Collodion Fetus, Lamellar Ichthyosis, LI, Lamellar Ichthyosis, Type 1, Ichthyosis Congenita II, ICR2, Self-Healing Collodion Baby,
  • Transglutaminase 1
    OMIM # 190195
    TGM1, Transglutaminase, Keratinocyte, TGK, Transglutaminase, Epidermal Type I,
  • Complex I, Subunit ND5
    OMIM # 516005
    MTND5, NADH-Ubiquinone Oxidoreductase, Subunit ND5, NADH Dehydrogenase, Subunit 5
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