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CTGA Database Listing
Arab Genomic Studies
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  • Paroxysmal Nonkinesigenic Dyskinesia 1
    OMIM # 118800
    PNKD1, Paroxysmal Dystonic Choreoathetosis, PDC, Choreoathetosis, Familial Paroxysmal, FPD1, Mount-Reback Syndrome, Choreoathetosis, Nonkinesigenic, Dystonia 8, DYT8
  • Chondrocalcinosis 2
    OMIM # 118600
    CCAL2, Chondrocalcinosis, Familial Articular, Calcium Gout, Calcium Pyrophosphate Arthropathy, Calcium Pyrophosphate Dihydrate Deposition Disease, CPPDD
  • Alagille Syndrome 1
    OMIM # 118450
    ALGS1, Alagille Syndrome, ALGS, Alagille-Watson Syndrome, AWS, Cholestasis with Peripheral Pulmonary Stenosis, Arteriohepatic Dysplasia, AHD, Hepatic Ductular Hypoplasia, Syndromatic
  • Chiari Malformation Type I
    OMIM # 118420
    CM1, Chiari Malformation Type I with Syringomyelia, CM1 with Syringomyelia
  • Cherubism
    OMIM # 118400
    CRBM
  • Cerebrocostomandibular Syndrome
    OMIM # 117650
    CCMS, Rib Gap Defects with Micrognathia,
  • ETHE1 Gene
    OMIM # 608451
    ETHE1, Hepatoma Subtracted Clone One, HSCO, D83198
  • Sotos Syndrome 1
    OMIM # 117550
    SOTOS1, Sotos Syndrome, Cerebral Gigantism, Chromosome 5q35 deletion syndrome
  • Multiple Acyl-CoA Dehydrogenation Deficiency
    OMIM # 231680
    MADD, Glutaric Acidemia II, Glutaric Aciduria II, GA II, Ethylmalonic-Adipicaciduria, EMA, Glutaric Acidemia IIA, ETFA Deficiency, Glutaric Acidemia IIB, ETFB Deficiency, Glutaric Acidemia IIC, ETFDH Deficiency
  • Methyl-CpG Binding Protein 2
    OMIM # 300005
    MECP2
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