Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2571 Sort by:
  • Hypothyroidism, Congenital, Nongoitrous, 2
    OMIM # 218700
    CHNG2, Thyroid Dysgenesis, Thyroid Agenesis, Thyroid Hypoplasia, Thyroid, Ectopic, Hypothyroidism, Congenital, due to Thyroid Dysgenesis, Hypothyroidism, Athyreotic, Athyreotic Hypothyroidism, Resistance to Thyrotropin, RTSH, Thyrotropin Resistance
  • Extracellular Matrix Protein 1
    OMIM # 602201
    ECM1
  • Lipoid Proteinosis of Urbach and Wiethe
    OMIM # 247100
    Lipoproteinosis, Hyalinosis Cutis et Mucosae, Urbach Wiethe Disease
  • Craniofacial Dyssynostosis with Short Stature
    OMIM # 218350
    Bilateral Lambdoid and Sagittal Synostosis, BLSS
  • Apparent Mineralocorticoid Excess
    OMIM # 218030
    Cortisol 11-Beta-Ketoreductase Deficiency, AME, AME1, 11-@Beta-Hydroxysteroid Dehydrogenase, Type II, HSD11B2, 11-@Beta-HSD, HSD11, Kidney and Placental Type, HSD11K, HSD11, Type II
  • Corpus Callosum, Agenesis of
    OMIM # 217990
    ACC
  • Corneal Endothelial Dystrophy
    OMIM # 217700
    CHED, Corneal Dystrophy, Congenital Hereditary Endothelial, Congenital Hereditary Endothelial Dystrophy of Cornea, Maumenee Corneal Dystrophy, Corneal Endothelial Dystrophy 2, Autosomal Recessive, CHED2
  • Cornea Plana 2
    OMIM # 217300
    CAN2
  • Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3
    OMIM # 604292
    EEC3
  • Tumor Protein p63
    OMIM # 603273
    TP63, Tumor Protein p73-Like, TP73L, p53-Related Protein p63, p63, KET
  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. >>