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CTGA Database Listing
Arab Genomic Studies
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  • Epilepsy, Nocturnal Frontal Lobe, 1
    OMIM # 600513
    ENFL1, Autosomal Dominant Nocturnal Frontal Lobe Epilepsy, ADNFLE,
  • Enterocolitis
    OMIM # 226150
    Necrotizing Enterocolitis
  • Neurofibromatosis, Type II
    OMIM # 101000
    NF2, Neurofibromatosis, Central Type, Acoustic Schwannomas, Bilateral, Bilateral Acoustic Neurofibromatosis, BANF, Acoustic Neurinoma, Bilateral, ACN
  • Ectodermal Dysplasia 8, Hair/Tooth/Nail Type
    OMIM # 602401
    ECTD8, Fried's Tooth and Nail Syndrome,
  • Achondroplasia
    OMIM # 100800
    ACH
  • Ectodermal Dysplasia and Neurosensory Deafness
    OMIM # 224800
  • Clouston Syndrome
    OMIM # 129500
    Ectodermal Dysplasia 2, Closuton Type, ECTD2, Ectodermal Dysplasia, Hidrotic, Autosomal Dominant, Closutin Hidrotic Ectodermal Dysplasia, Ectodermal Dysplasia, Hidrotic, 2, HED2,
  • Gap Junction Protein, Beta-6
    OMIM # 604418
    GJB6, Connexin 30, CX30,
  • Adams-Oliver Syndrome 1
    OMIM # 100300
    AOS1, Absence Defect of Limbs, Scalp, and Skull , AOS, Aplasia Cutis Congenita with Terminal Transverse Limb Defects, Congenital Scalp Defects with Distal Limb Reduction Anomalies
  • Ectodermal Dysplasia 10B, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
    OMIM # 224900
    ECTD10B, Ectodermal Dysplasia, Hypohidrotic, HED, Ectodermal Dysplasia, Anhidrotic, EDA,
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