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CTGA Database Listing
Arab Genomic Studies
Records found: 2477 Sort by:
  • Hexosaminidase B
    OMIM # 606873
    HEXB, ENC1, Antisense, ENC1AS
  • Sandhoff Disease
    OMIM # 268800
    GM2-Gangliosidosis, Type II, Hexosaminidases A and B Deficiency, Sandhoff Disease, Adult Type, Sandhoff Disease, Juvenile Type, Sandhoff Disease, Infantile Type
  • RECQ Protein-Like 4
    OMIM # 603780
    RECQL4, DNA Helicase, RECQ-Like, Type 4, RECQ4
  • Rothmund-Thomson Syndrome
    OMIM # 268400
    RTS, Poikiloderma Atrophicans and Cataract
  • Cohen Syndrome
    OMIM # 216550
    COH1, CHH1, Hypotonia Obesity and Prominent Incisors, Pepper Syndrome, CHS1
  • Retinopathy, Pigmentary, and Mental Retardation
    OMIM # 268050
    Mirhosseini-Holmes-Walton Syndrome,
  • Vacuolar Protein Sorting 13, Yeast, Homolog of, B
    OMIM # 607817
    VPS13B, COH1 Gene, COH1, KIAA0532, ,
  • Laminin, Alpha-3
    OMIM # 600805
    LAMA3, Laminin A3, Laminin 5, Alpha-3 Subunit, LAM5, Alpha-3 Subunit, Epiligrin, 170-kd Subunit, BM600
  • Epidermolysis Bullosa, Junctional, Herlitz Type
    OMIM # 226700
    Epidermolysis Bullosa Junctionalis, Herlitz Type, JEB-Herlitz Type, Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type, Herlitz-Pearson-Type Epidermolysis Bullosa, Epidermolysis Bullosa Letalis
  • Microcephaly 5, Primary, Autosomal Recessive
    OMIM # 608716
    MCPH5
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