Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Seizures, Scoliosis, and Macrocephaly/Microcephaly Syndrome
    OMIM # 616682
    SSMS
  • Exostosin Glycosyltransferase 2
    OMIM # 608210
    EXT2, Exostosin 2
  • Diabetes Insipidus, Neurohypophyseal Type
    OMIM # 125700
    Diabetes Insipidus, Primary Central, CDI, Diabetes Insipidus, Cranial Type,
  • Arginine Vasopressin
    OMIM # 192340
    AVP, ARVP, Vasopressin-Neurophysin II, Antidiuretic Hormone, ADH, Neurophysin II, NPII,
  • Congenital Disorder of Glycosylation, Type IIn
    OMIM # 616721
    CDG2N, CDG IIn, CDGIIn
  • 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
  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. >>