Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2749 Sort by:
  • Dermatopontin
    OMIM # 125597
    DPT
  • Forkhead Box C1
    OMIM # 601090
    FOXC1, Forkhead, Drosophila, Homolog-Like 7, FKHL7, Forkhead-Related Activator 3, FREAC3
  • Anterior Segment Dysgenesis 3
    OMIM # 601631
    ASGD3, Iridiogoniodysgenesis, Type 1, IRID1, Iridogoniodysgenesis Anomaly, Autosomal Dominant, IGDA, Iris Hypoplasia with Glaucoma, Glaucoma iridogoniodesplasia, Familial
  • Charcot-Marie-Tooth Disease, X-Linked Dominant, 1
    OMIM # 302800
    CMTX1, CMTX, Charcot-Marie-Tooth Peroneal Muscular Atrophy, X-Linked, Hereditary Motor and Sensory Neuropathy, X-Linked, HMSN, X-Linked, Charcot-Marie-Tooth Neuropathy, X-Linked, 1, CMT2
  • Gap Junction Protein, Beta-1
    OMIM # 304040
    GJB1, Gap Junction Protein, 32-KD, Connexin 32, CX32, Liver Connexin
  • Cerebral Creatine Deficiency Syndrome 1
    OMIM # 300352
    CCDS1, Creatine Deficiency Syndrome, X-Linked, Creatine Transporter Defect, Mental Retardation, X-Linked, with Seizures, Short Stature, and Midface Hypoplasia, Mental Retardation, X-Linled, with Creatine Transport Deficiency,
  • Solute Carrier Family 6 (Neurotransmitter Transporter, Creatine), Member 8
    OMIM # 300036
    SLC6A8, Creatine Transporter, CT1, CRTR, CRT
  • Muscular Dystrophy, Duchenne Type
    OMIM # 310200
    DMD, Duchenne Muscular Dystrophy, Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
  • Dystrophin
    OMIM # 300377
    Apo-Dystrophin 1
  • Nephrotic Syndrome, Type 4
    OMIM # 256370
    NPHS4,
  1. <<
  2. ...
  3. 11
  4. 12
  5. 13
  6. 14
  7. 15
  8. 16
  9. 17
  10. 18
  11. 19
  12. 20
  13. 21
  14. 22
  15. ...
  16. >>