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CTGA Database Listing
Arab Genomic Studies
Records found: 2744 Sort by:
  • Renal Tubular Dysgenesis
    OMIM # 267430
    RTD, Primitive Renal Tubule Syndrome, Renal Tubular Dysgenesis with Choanal Atresia and Athelia
  • Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness
    OMIM # 267300
    Renal Tubular Acidosis with Progressive Nerve Deafness, RTA with Progressive Nerve Deafness, Renal Tubular Acidosis, Autosomal Recessive, with Progressive Nerve Deafness, dRTA and Sensorineural Deafness
  • Short-Rib Thoracic Dysplasia 9 with or without Polydactyly
    OMIM # 266920
    SRTD9, Mainzer-Saldino Syndrome, MZSDS, Conorenal Syndrome, Renal Dysplasia, Retinal Pigmentary Dystrophy, Cerebellar Ataxia, and Skeletal Dysplasia,
  • Senior-Loken Syndrome 1
    OMIM # 266900
    SLSN1, Senior-Loken Syndrome, Loken-Senior Syndrome, Renal-Retinal Syndrome, Juvenile Nephronophthisis with Leber Amaurosis, Renal Dysplasia and Retinal Aplasia
  • Ataxia-Telangiectasia-Like Disorder
    OMIM # 604391
    ATLD
  • Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders
    OMIM # 604363
  • Microcephaly 2, Primary, Autosomal Recessive, with or without Cortical Malformations
    OMIM # 604317
    MCPH2
  • Cataract, Coppock-Like
    OMIM # 604307
    CCL, Cataract, Embryonic Nuclear
  • Rheumatoid Arthritis, Systemic Juvenile
    OMIM # 604302
    Systemic Juvenile Rheumatoid Arthritis, Juvenile Rheumatoid Arthritis, JRA, Juvenile Chronic Arthritis, JCA, Juvenile Idiopathic Arthritis, JIA
  • Pyruvate Kinase Deficiency of Red Cells
    OMIM # 266200
    Pyruvate Kinase Deficiency of Erythrocyte , PK Deficiency
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