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CTGA Database Listing
Arab Genomic Studies
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  • Pyruvate Kinase Deficiency of Red Cells
    OMIM # 266200
    Pyruvate Kinase Deficiency of Erythrocyte , PK Deficiency
  • Pyloric Atresia
    OMIM # 265950
    Congenital Pyloric Atresia, CPA,
  • Pulmonary Alveolar Microlithiasis
    OMIM # 265100
    PAM
  • Progeroid Syndrome, Neonatal
    OMIM # 264090
    Wiedemann-Rautenstrauch Syndrome, Neonatal Pseudo-Hydrocephalic Progeroid Syndrome of Wiedemann-Rautenstrauch , Rautenstrauch-Wiedemann Type Neonatal Progeria, Rautenstrauch-Wiedemann Syndrome,
  • PKHD1
    OMIM # 606702
    Fibrocystin, FCYT, Polyductin, Polycystic Kidney and Hepatic Disease 1 Gene
  • Polycystic Kidney Disease 4 with or without Polycystic Liver Disease
    OMIM # 263200
    PKD4, Polycystic Kidney Disease 4 with or without Hepatic Disease, Polycystic Kidney Disease, Autosomal Recessive, ARPKD, Polycystic Kidney and Hepatic Disease 1, PKHD1, Polycystic Kidney Disease, Infantile, Type I, PKD3
  • T Cell Immune Regulator 1
    OMIM # 604592
    TCIRG1, ATPase, H+ Transporting, Lysosomal, V0 Subunit A, Isoform 3, Vacuolar Proton Pump, Alpha Subunit 3, TIRC7, OC116, ATPase, H+ Transporting, Lysosomal, V0 Subunit A3, ATP6V0A3
  • Osteopetrosis, Autosomal Recessive 1
    OMIM # 259700
    OPTB1, Marble Bones, Autosomal Recessive, Albers-Schonberg Disease, Autosomal Recessive, Osteopetrosis, Malignant, Osteopetrosis, Infantile Malignant 1
  • Orofaciodigital Syndrome, Type IV
    OMIM # 258860
    OFD4, OFD Syndrome IV, Oral-Facial-Digital Syndrome, Type IV, OFD Syndrome, Baraitser-Burn Type, OFD Syndrome with Tibial Defects, Baraitser-Burn Syndrome, Mohr-Majewski Syndrome
  • Odontoonychodermal Dysplasia
    OMIM # 257980
    OODD, Fadhil Syndrome
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