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CTGA Database Listing
Arab Genomic Studies
Records found: 2247 Sort by:
  • Ichthyosis, Congenital, Autosomal Recessive 4A
    OMIM # 601277
    ARCI4A, Ichthyosis Congenita IIB, ICR2B, Ichthyosis, Lamellar, 2, LI2,
  • Ectodermal Dysplasia 1, Hypohidrotic, X-Linked
    OMIM # 305100
    XHED, Ectodermal Dysplasia 1, Hypohidrotic/Hair/Tooth Type, X-Linked, ECTD1, XLHED, Ectodermal Dysplasia, Anhidrotic, X-Linked, EDA, EDA1, Ectodermal Dysplasia, Hypohidrotic, 1, HED1, Ectodermal Dysplasia 1, ED1, Christ-Siemens-Touraine Syndrome, CST Syndrome,
  • Ectodysplasin A
    OMIM # 300451
    EDA, Ectodysplasin, EDA1 Gene, ED1 Gene, ED1, Ectodysplasin A1 Isoform, EDA-A1, Ectodysplasin A2 Isoform, EDA-A2,
  • Parathyroid Hormone 1 Receptor
    OMIM # 168468
    PTH1R, Parathyroid Hormone Receptor 1, PTHR1, PTH Receptor, PTHR, Parathyroid Hormone/Parathyroid Hormone-Related Protein Receptor, PTH/PTHRP Receptor,
  • Macrophage Migration Inhibitory Factor
    OMIM # 153620
    MIF, MMIF,
  • Neu-Laxova Syndrome 1
    OMIM # 256520
    Neu-Laxova Syndrome; NLS
  • Microvascular Complications of Diabetes, Susceptibility to, 1
    OMIM # 603933
    Proliferative Retinopathy, Diabetic, Susceptibility to, Nonproliferative Retinopathy, Diabetic, Susceptibility to, Microvascular Complications of Diabetes, Susceptibility to, Microvascular Complications of Diabetes, Protection from, Nephropathy, Diabetic, Susceptibility to, End-Stage Renal Disease, Diabetic, Susceptibility to, Proliferative Retinopathy, Diabetic, Susceptibility to, Nonproliferative Retinopathy, Diabetic, Susceptibility to, Neuropathy, Diabetic, Susceptibility to
  • Cardiomyopathy, Dilated, 1A
    OMIM # 115200
    CMD1A, Cardiomyopathy, Dilated, with Conduction Defect 1, CDCD1, Cardiomyopathy, Idiopathic Dilated, Cardiomyopathy, Familial Idiopathic, Cardiomyopathy, Congestive, IDC
  • Protein C
    OMIM # 612283
    PROC, PC,
  • Thrombophilia Due to Protein C Deficiency, Autosomal Recessive
    OMIM # 612304
    THPH4, Protein C Deficiency, Autosomal Recessive, PROC Deficiency, Autosomal Recessive,
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