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CTGA Database Listing
Arab Genomic Studies
Records found: 2512 Sort by:
  • Failure of Tooth Eruption, Primary
    OMIM # 125350
    Primary Failure of Eruption, Nonsyndromic, Primary Retention of Teeth, Unerupted Second Primary Molar, Posterior Openbite Malocclusion, Familial, Dental Noneruption,
  • Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy
    OMIM # 125310
    CADASIL, Dementia, Hereditary Multi-Infarct Type, CASIL, Chronic Familial Vascular Encephalopathy, Familial Disorder with Subcortical Ischemic Strokes, Agnogenic Medial Arteriopathy, Familial Binswanger's Disease
  • Vohwinkel Syndrome
    OMIM # 124500
    VOWNKL, Deafness, Congenital, with Keratopachydermia and Constrictions of Fingers and Toes, Mutilating Keratoderma, Keratoderma Hereditarium Mutilans, KHM
  • Darier-White Disease
    OMIM # 124200
    DAR, Keratosis Follicularis, Darier Disease, DD, Darier Disease, Acral Hemorrhagic Type, Darier Disease, Segmental,,
  • Mitochondrial Complex III Deficiency, Nuclear Type 1 (*)
    OMIM # 124000
    MC3DN1
  • Crouzon Syndrome
    OMIM # 123500
    Craniofacial Dysostosis, Type I, CFD1, Crouzon Craniofacial Dysostosis
  • Cri-Du-Chat Syndrome
    OMIM # 123450
    Cat Cry Syndrome, Chromosome 5p Deletion Syndrome
  • Creutzfeldt-Jakob Disease
    OMIM # 123400
    CJD, Creutzfeldt-Jakob Disease, Familial, Creutzfeldt-Jakob Disease, Sporadic, sCJD, Creutzfeldt-Jakob Disease, Variant, vCJD, Creutzfeldt-Jakob Disease, Heidenhain Variant
  • Cornelia de Lange Syndrome 1
    OMIM # 122470
    CDLS1, CDL, CDLS, Typus Degenerativus Amstelodamensis, De Lange Syndrome, Brachmann-de Lange Syndrome, BDLS
  • Schnyder Corneal Dystrophy
    OMIM # 121800
    SCCD, Crystalline Stromal Dystrophy, Hereditary Crystalline Stromal Dystrophy of Schnyder, SCD, Schnyder Crystalline Corneal Dystrophy, Schnyder Crystalline Dystrophy Sine Crystals,
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