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CTGA Database Listing
Arab Genomic Studies
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  • Shprintzen-Goldberg Craniosynostosis Syndrome
    OMIM # 182212
    SGS, Craniosynostosis with Arachnodactyly and Abdominal Hernias, Marfanoid Disorder with Craniosynostosis, Type I, Marfanoid Craniosynostosis Syndrome
  • Scoliosis, Isolated, Susceptibility to, 1
    OMIM # 181800
    IS1, Adolescent Isolated Scoliosis, AIS, Adolescent Idiopathic Scoliosis
  • Familial Progressive Scleroderma
    OMIM # 181750
    Systemic Sclerosis, Susceptibility to
  • Schizophrenia
    OMIM # 181500
    SCZD, Schizoaffective Disorder
  • Salivary Gland Adenoma, Pleomorphic
    OMIM # 181030
    SGPA, PSA
  • Sarcoidosis, Susceptibility to, 1
    OMIM # 181000
    SS1, Sarcoidosis, Sarcoid Disease, Boeck Sarcoid, Besnier-Boeck-Schaumann Disease
  • Silver-Russell Syndrome
    OMIM # 180860
    SRS, Russell-Silver Syndrome, RSS, Silver-Russell Dwarfism,
  • Rubinstein-Taybi Syndrome 1
    OMIM # 180849
    RSTS1, RSTS, Rubinstein Syndrome, Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation, Broad Thumb-Hallux Syndrome
  • Axenfeld-Rieger Syndrome, Type 1
    OMIM # 180500
    Rieger Syndrome, Type 1, RIEG1, RIEG, RGS, Iridogoniodysgenesis with Somatic Anomalies
  • Rheumatoid Arthritis
    OMIM # 180300
    RA
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