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CTGA Database Listing
Arab Genomic Studies
Records found: 2614 Sort by:
  • Papillon-Lefevre Syndrome
    OMIM # 245000
    PALS, PLS, Keratosis Palmoplantaris with Periodontopathia
  • Paget Disease of bone 2, Early-onset
    OMIM # 602080
    PDB2
  • Kaposi Sarcoma
    OMIM # 148000
    Multiple Idiopathic Pigmented Hemangiosarcoma, Susceptibility to, Multicentric Castleman Disease, Susceptibility to
  • Osteopetrosis-Associated Transmembrane Protein 1
    OMIM # 607649
    OSTM1, Grey-Lethal, Mouse, Homolog of, GL
  • Osteopetrosis, Autosomal Recessive 5
    OMIM # 259720
    OPTB5, Osteopetrosis, Infantile Malignant 3
  • Osteopetrosis, Autosomal Recessive 1
    OMIM # 259700
    OPTB1, Marble Bones, Autosomal Recessive, Albers-Schonberg Disease, Autosomal Recessive, Osteopetrosis, Malignant, Osteopetrosis, Infantile Malignant 1
  • Oculodentodigital Dysplasia, Autosomal Recessive
    OMIM # 257850
    ODDD, Autosomal Recessive, Oculodentoosseous Dysplasia, Autosomal Recessive, ODOD, Autosomal Recessive
  • Night Blindness, Congenital Stationary, Type 1E
    OMIM # 614565
    CSNB1E, CSNB, Complete, Autosomal Recessive
  • G Protein-Coupled Receptor 179
    OMIM # 614515
    GPR179, GPR158-Like, GPR158L, GPR158L1
  • Neurofaciodigitorenal Syndrome
    OMIM # 256690
    NFDR Syndrome
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