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CTGA Database Listing
Arab Genomic Studies
Records found: 2507 Sort by:
  • Caffey Disease
    OMIM # 114000
    Infantile Cortical Hyperostosis, Prenatal Cortical Hyperostosis, Lethal,
  • Burkitt Lymphoma
    OMIM # 113970
    BL
  • Epidermolytic Hyperkeratosis
    OMIM # 113800
    EHK, Bullous Erythroderma Ichthyosiformis Congenita of Brocq, Bullous Congenital Ichthyosiform Erythroderma, BCIE, Bullous Ichthyosiform Erythroderma, BIE, Epidermolytic Ichthyosis, Epidermolytic Hyperkeratosis, Late-Onset
  • Branchiooculofacial Syndrome
    OMIM # 113620
    BOF Syndrome, BOFS, Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging, Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome, Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome, Lee Root Fenske Syndrome
  • Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia
    OMIM # 113610
  • Branchial Cleft Anomalies
    OMIM # 113600
    Branchial Cysts, Lateral Cervical Anomaly
  • Brachydactyly-Nystagmus-Cerebellar Ataxia
    OMIM # 113400
    Biemond Syndrome
  • Brachydactyly, Type B1
    OMIM # 113000
    BDB1, Brachydactyly, Type B, BDB
  • Blepharophimosis, Ptosis, and Epicanthus Inversus
    OMIM # 110100
    BPES, BPES, Type I, BPES, Type II, BPES with Ovarian Failure , BPES without Ovarian Failure, BPES with Duane Retraction Syndrome
  • Bladder Cancer
    OMIM # 109800
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