Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2441 Sort by:
  • Morquio Syndrome A
    OMIM # 253000
    Mucopolysaccharidosis Type IVA, MPS IVA, MPS4A, Morquio A Disease, Galactosamine-6-Sulfatase Deficiency, GALNS Deficiency
  • Achalasia-Addisonianism-Alacrima Syndrome
    OMIM # 231550
    AAA, Triple-A Syndrome, Alacrima-Achalasia-Adrenal Insufficiency Neurologic Disorder, Glucocorticoid Deficiency and Achalasia, Allgrove Syndrome, Addisonian-Achalasia Syndrome, Hypoadrenalism with Achalasia, Alacrima-Achalasia-Addisonianism, Acth-Resistant Adrenal Insufficiency, Achalasia and Alacrima, Achalasia-Alacrima Syndrome,
  • Autism
    OMIM # 209850
    Autistic Disorder
  • Duane Retraction Syndrome 1
    OMIM # 126800
    DURS1, DRS, Duane Syndrome, DUS, Duane Anomaly, Retraction Syndrome
  • Carbonic Anhydrase VIII
    OMIM # 114815
    CA8, CA VIII, Carbonic Anhydrase-Related Polypeptide, CARP, Carbonic Anhydrase-Like Sequence, CALS
  • Aniridia
    OMIM # 106210
    AN, Aniridia II, AN2
  • WD Repeat-Containing Protein 45B
    OMIM # 609226
    WDR45B
  • Toll-Like Receptor 2
    OMIM # 603028
    TLR2, Toll/Interleukin 1 Receptor-Like 4, TIL4
  • Spastic Ataxia 1, Autosomal Dominant
    OMIM # 108600
    SPAX1
  • Vesicle-Associated Membrane Protein 1
    OMIM # 185880
    VAMP1, Synaptobrevin 1, SYB1
  1. <<
  2. ...
  3. 5
  4. 6
  5. 7
  6. 8
  7. 9
  8. 10
  9. 11
  10. 12
  11. 13
  12. 14
  13. 15
  14. 16
  15. ...
  16. >>