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CTGA Database Listing
Arab Genomic Studies
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  • Surfactant Metabolism Dysfunction, Pulmonary, 1
    OMIM # 265120
    SMDP1, Pulmonary Alveolar Proteinosis, Congenital, 1, Interstitial Lung Disease due to Surfactant Protein B Deficiency, Interstitial Lung Disease, Nonspecific, due to Surfactant Protein B Deficiency
  • Surfactant, Pulmonary-Associated Protein B
    OMIM # 278640
    SFTPB, Surfactant-Associated Protein, Pulmonary, 3, SFTP3, Pulmonary Surfactant Apoprotein PSP-B, SPB, PSP-B, Pulmonary Surfactant-Associated Protein, 18-KD,
  • Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 Chondrodysplasia Punctata with Coagulation Factor Deficiency
    OMIM # 277450
    VKCFD1, VKCFD, Vitamin K-Dependent Coagulation Defect, Familial Multiple Coagulation Factor Deficiency III, FMFD III, Multiple Coagulation Factor Deficiency III, MCFD3, Factors II, VII, IX, and X, Combined Deficiency of, Glutamic Acid, Deficient Gamma-Carboxylation of
  • Gamma-Glutamyl Carboxylase
    OMIM # 137167
    GGCX
  • Afibrinogenemia, Congenital
    OMIM # 202400
    Hypofibrinogenemia, Congenital,
  • Fibrinogen, G Gamma Polypeptide
    OMIM # 134850
    FGG, Fibrinogen--Gamma Polypeptide Chain
  • Amelogenesis Imperfecta Type IB
    OMIM # 104500
    AI1B, Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant, AIH2, Enamel Hypoplasia, Hereditary Localized
  • Enamelin
    OMIM # 606585
    ENAM
  • Lujan-Fryns Syndrome
    OMIM # 309520
    Mental Retardation, X-Linked, with Marfanoid Habitus
  • OCRL Gene
    OMIM # 300535
    OCRL, OCRL1
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