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CTGA Database Listing
Arab Genomic Studies
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  • Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1
    OMIM # 224050
    CAMRQ1, Cerebellar Hypoplasia, VLDLR-Associated, Cerebellar Ataxia and Mental Retardation with or without Quadrupedal Locomotion 1, Cerebellar Ataxia, Congenital, and Mental Retardation, Autosomal Recessive, Dysequilibrium Syndrome, DES
  • F-Box Only Protein 32
    OMIM # 606604
    FBXO32, Muscle Atrophy F-Box, MAFBX, Atrophy Gene 1, ATROGIN1, FLJ32424,
  • Chondrodysplasia, Grebe Type
    OMIM # 200700
    Achondrogenesis, Brazilian, Grebe Chondrodysplasia, Grebe Dysplasia, Acromesomelic Dysplasia, Grebe Type, AMDG, Achondrogenesis, Type II, Formerly,
  • Growth/Differentiation Factor 5
    OMIM # 601146
    GDF5, Cartilage-Derived Morphogenetic Protein 1, CDMP1, Lipopolysaccharide-Associated Protein 4, LAP4, LPS-Associated Protein 4, Bone Morphogenetic Protein 14, BMP14,
  • Retinitis Pigmentosa 80
    OMIM # 617781
    RP80
  • Intraflagellar Transport 140, Chlamydomonas, Homolog of
    OMIM # 614620
    IFT140, KIAA0590,
  • Low Density Lipoprotein Receptor-Related Protein 2
    OMIM # 600073
    LRP2, Glycoprotein 330, Megalin
  • Donnai-Barrow Syndrome
    OMIM # 222448
    Faciooculoacoudticorenal Syndrome, DBS/FOAR Syndrome, Diaphragmatic Hernia, Exomphalos, Absent Corpus Callosum, Hypertelorism, Myopia, Sensorineural Deafness, and Proteinuria
  • Proprotein Convertase, Subtilisin/Kexin-Type, 1
    OMIM # 162150
    PCSK1, Neuroendocrine Convertase 1, NEC1, Proprotein Convertase 1, PC1, Prohormone Convertase 1, Prohormone Convertase 3, PC3
  • Proprotein Convertase 1/3 Deficiency
    OMIM # 600955
    Obesity and Endocrinopathy due to Impaired Proessing of Prohormones
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