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CTGA Database Listing
Arab Genomic Studies
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  • Pfeiffer Syndrome
    OMIM # 101600
    Acrocephalosyndactyly, Type V, ACS5, ACS V, Noack Syndrome, Craniofacial-Skeletal-Dermatologic Dysplasia
  • Saethre-Chotzen Syndrome
    OMIM # 101400
    SCS, Acrocephalosyndactyly, Type III, ACS3, ACS III, Chotzen Syndrome, Acrocephaly, Skull Asymmetry, and Mild Syndactyly, Saethre-Chotzen Syndrome with Eyelid Anomalies, Blepharophimosis, Epicanthus Inversus, and Ptosis 3, BPES3,
  • Apert Syndrome
    OMIM # 101200
    Acrocephalosyndactyly, Type I , ACS1, ACS I, Apert-Crouzon Disease, Acrocephalosyndactyly, Type II, ACS II, VOGT Cephalodactyly, Apert-Like Polydactyly Syndrome,
  • Neurofibromatosis, Type II
    OMIM # 101000
    NF2, Neurofibromatosis, Central Type, Acoustic Schwannomas, Bilateral, Bilateral Acoustic Neurofibromatosis, BANF, Acoustic Neurinoma, Bilateral, ACN
  • Achondroplasia
    OMIM # 100800
    ACH
  • Cholinergic Receptor, Nicotinic, Gamma Polypeptide
    OMIM # 100730
    CHRNG, Acetylcholine Receptor, Muscle, Gamma Subunit, ACHRG
  • Adams-Oliver Syndrome
    OMIM # 100300
    Absence Defect of Limbs, Scalp, and Skull , AOS, Aplasia Cutis Congenita with Terminal Transverse Limb Defects, Aplasia Cutis Congenita, Congenital Heart Defect, and Frontonasal Cysts, Congenital Scalp Defects with Distal Limb Reduction Anomalies
  • Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism
    OMIM # 100100
    Prune Belly Syndrome, Eagle-Barrett Syndrome, EGBRS,
  • Zellweger Syndrome
    OMIM # 214100
    ZS, Cerebrohepatorenal Syndrome, CHR Syndrome, ZWS, Peroxisome Biogenesis Disorder, ZS, PBD, ZS, Bowen Syndrome
  • Young Syndrome
    OMIM # 279000
    Azoospermia, Obstructive, and Chronic Sinopulmonary Infections, Sinusitis-Infertility Syndrome, Barry-Perkins-Young Syndrome,
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