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CTGA Database Listing
Arab Genomic Studies
Records found: 2881 Sort by:
  • Mucopolysaccharidosis Type VI
    OMIM # 253200
    MPS VI, MPS6, Maroteaux-Lamy Syndrome, Arylsulfatase B Deficiency, ARSB Deficiency, N-Acetylgalactosamine-4-Sulfatase Deficiency,
  • Mucopolysaccharidosis Type IIIB
    OMIM # 252920
    MPS IIIB, MPS3B, Sanfilippo Syndrome B, N-Acetyl-Alpha-D-Glucosaminidase Deficiency, NAGLU Deficiency, N-Acetylglucosaminidase, Alpha-, NAGLU, N-Acetyl-Alpha-D-Glucosaminidase Polymorphism, NAG Polymorphism,
  • Spinal Muscular Atrophy, Type I
    OMIM # 253300
    SMA I, SMA, Infantile Acute Form, Muscular Atrophy, Infantile, Werdnig-Hoffmann Disease,
  • Myasthenia Gravis
    OMIM # 254200
    MG
  • Nephronophthisis 1
    OMIM # 256100
    NPHP1, Nephronophthisis, Familial Juvenile, NPH1,
  • Meckel Syndrome, Type 1
    OMIM # 249000
    MKS1, Meckel Syndrome, MKS, MES, Dysencephalia Splanchnocystica, Gruber Syndrome, Meckel-Gruber Syndrome, Meckel-Gruber Syndrome, Type 1
  • MKS1 Gene
    OMIM # 609883
    MKS1, FLJ20345, BBS13 Gene
  • Plectin
    OMIM # 601282
    PLEC, PLEC1, PCN, PLTN
  • Postmeiotic Segregation Increased, S. Cerevisiae, 2
    OMIM # 600259
    PMS2, Mismatch Repair Gene PMSL2, PMSL2
  • Cadherin 1
    OMIM # 192090
    CDH1, Cadherin, Epithelial, E-Cadherin, CDHE, ECAD, Uvomorulin, UVO, Calcium-Dependent Adhesion Protein, Epithelial, Liver Cell Adhesion Molecule, LCAM
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