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CTGA Database Listing
Arab Genomic Studies
Records found: 2614 Sort by:
  • Lipodystrophy, Congenital Generalized, Type 2
    OMIM # 269700
    CGL2, Berardinelli-Seip Congenital Lipodystrophy Type 2, Seip Syndrome, Berardinelli Syndrome, Lipodystrophy, Total, and Acromegaloid Gigantism, Congenital Lipoatrophic Diabetes, Lipodystrophy, Berardinelli-Seip Congenital Type 2, Brunzell Syndrome, Brunzell Syndrome, BSCL2-Related
  • SHORT Syndrome
    OMIM # 269880
    Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly, and Teething Delay, Lipodystrophy, Partial, With Rieger Anomaly, and Short Stature
  • Sjogren Syndrome
    OMIM # 270150
    Sicca Syndrome
  • Sjogren-Larsson Syndrome
    OMIM # 270200
    SLS, Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia, Fatty Alcohol:NAD+ Oxidoreductase Deficiency, FAO Deficiency, Fatty Aldehyde Dehydrogenase Deficiency, FALDH Deficiency, Aldehyde Dehydrogenase, Family 3, Subfamily A, Member 2, ALDH3A2, Aldehyde Dehydrogenase 10, ALDH10, Fatty Aldehyde Dehydrogenase , FALDH,
  • Diarrhea 3, Secretory Sodium, Congenital, with or without Other Congenital Anomalies
    OMIM # 270420
    DIAR3, Sodium Diarrhea, Congenital, CSD, Diarrhea 3, Secretory Sodium, Congenital, Syndromic
  • Spastic Diplegia, Infantile Type
    OMIM # 270600
  • Spastic Paraplegia 23
    OMIM # 270750
    SPG23, Spastic Paraplegia with Pigmentary Abnormalities, Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies, Lison Syndrome,
  • Spastic Paraplegia 5A, Autosomal Recessive
    OMIM # 270800
    SPG5A
  • Spastic Quadriplegia, Retinitis Pigmentosa, and Mental Retardation
    OMIM # 270950
  • Spinocerebellar Ataxia with Dysmorphism
    OMIM # 271270
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