Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2507 Sort by:
  • Dyssegmental Dysplasia, Rolland-Desbuquois Type
    OMIM # 224400
    DDRD, Dyssegmental Dwarfism, Rolland-Desbuquois Type, Anisospondylic Camptomicromelic Dwarfism, Rolland-Desbuquois Type
  • Hydrocephalus, congenital, 1
    OMIM # 236600
    Hydrocephaly, Ventriculomegaly, Hydrocephalus, nonsyndromic, autosomal recessive 1
  • Dyssegmental Dysplasia, Silverman-Handmaker Type
    OMIM # 224410
    DDSH, Dyssegmental Dwarfism, Silverman-Handmaker Type, Anisospondylic Camptomicromelic Dwarfism, Silverman-Handmaker Type
  • Hypergonadotropic Hypogonadism with Partial Alopecia
    OMIM # 241090
    Al Awadi Farag Teebi Syndrome
  • Hypoplastic Left Heart Syndrome 1
    OMIM # 241550
    HLHS1
  • Alternating Hemiplegia of Childhood 1
    OMIM # 104290
    AHC1
  • Alport Syndrome 3, Autosomal Dominant
    OMIM # 104200
    ATS3
  • Alopecia Areata 1
    OMIM # 104000
    AA1, Alopecia Universalis, AU
  • Hypoglossia-Hypodactylia
    OMIM # 103300
    Peromelia with Micrognathism, Oromandibular Limb Hypoplasia, Aglossia-Adactylia, Hanhart Syndrome
  • Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, due to Adenosine Deaminase Deficiency
    OMIM # 102700
    SCID due to ADA Deficiency , ADA-SCID, SCID due to ADA Deficiency, Early-Onset,
  1. <<
  2. ...
  3. 8
  4. 9
  5. 10
  6. 11
  7. 12
  8. 13
  9. 14
  10. 15
  11. 16
  12. 17
  13. 18
  14. 19
  15. ...
  16. >>