Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2741 Sort by:
  • Solute Carrier Family 39 (Zinc Transporter), Member 8
    OMIM # 608732
    SLC39A8, BIGM103, ZIP8
  • Apolipoprotein B
    OMIM # 107730
    APOB, APOB100, APOB48 , Apolipoprotein B-100, Apolipoprotein B48
  • Hypobetalipoproteinemia, Familial, 1
    OMIM # 615558
    FHBL1 , Hypobetalipoproteinemia, Familial, FHBL, Acanthocytosis with Hypobetalipoproteinemia, Hypobetalipoproteinemia, Normotriglyceridemic
  • Infantile Liver Failure Syndrome 2
    OMIM # 616483
    ILFS2
  • MAP7 Domain-Containing Protein 3
    OMIM # 300930
    MAP7D3
  • Major Affective Disorder 1
    OMIM # 125480
    MAFD1, Manic-Depressive Psychosis, MD1, Bipolar Affective Disorder, BPAD, Manic-Depressive Psychosis, Autosomal,
  • Heterotaxy, Visceral, 1, X-Linked
    OMIM # 306955
    HTX1, Dextrocardia with Other Cardiac Malformations, Laterality, X-Linked, Situs Inversus, Complex Cardiac Defects, and Splenic Defects, X-Linked, Congenital Heart Defects, Multiple Types, 1, X-Linked, CHTD1
  • Zinc Finger Transcription Factor TRPS1
    OMIM # 604386
    TRPS1, TRPS1 Gene
  • Cysteine-and-Glycine-Rich Protein 1
    OMIM # 123876
    CSRP1, Cysteine-Rich Protein 1, CRP1, Cysteine-Rich Protein, CSRP, CRP
  • Diabetes Mellitus, Noninsulin-Dependent
    OMIM # 125853
    NIDDM, Diabetes Mellitus, Type II, T2D, Noninsulin-Dependent Diabetes Mellitus, Maturity-Onset Diabetes
  1. <<
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. 8
  10. 9
  11. 10
  12. 11
  13. 12
  14. 13
  15. ...
  16. >>