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CTGA Database Listing
Arab Genomic Studies
Records found: 2507 Sort by:
  • Osteopetrosis, Autosomal Recessive 8
    OMIM # 615085
    OPTB8
  • Sorting Nexin 10
    OMIM # 614780
    OPTB8
  • Cytochrome P450, Subfamily I, Polypeptide 1
    OMIM # 601771
    CYP1B1, P4501B1
  • Piezo-Type Mechanosensitive Ion Channel Component 2
    OMIM # 613629
    PIEZO2, Family with Sequence Similarity 38, Member B, FAM38B,
  • Arthrogryposis, Distal, Type 3
    OMIM # 114300
    Gordon Syndrome, DA3, Arthrogryposis Multiplex Congenita, Distal, Type IIA, Camptodactyly, Cleft Palate, and Clubfoot
  • Campomelic Dysplasia
    OMIM # 114290
    CMPD, CMD1, CMPD1, CMPD1/SRA1, Campomelic Dysplasia with Autosomal Sex Reversal, Acampomelic Campomelic Dysplasia, Acampomelic Campomelic Dysplasia with Autosomal Sex Reversal, Camptomelic Dysplasia
  • 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
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