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CTGA Database Listing
Arab Genomic Studies
Records found: 2616 Sort by:
  • Steroid 5-Alpha-Reductase 2
    OMIM # 607306
    SRD5A2
  • Pseudovaginal Perineoscrotal Hypospadias
    OMIM # 264600
    PPSH, Male Pseudohermaphroditism due to 5-Alpha-Reductase Deficiency, Familial Incomplete Male Pseudohermaphroditism, Type 2, 5-Alpha-Reductase 2 Deficiency
  • Prolidase Deficiency
    OMIM # 170100
  • POF1B Gene
    OMIM # 300603
    POF1B, FLJ22792, Actin-Binding Protein, 34-KD
  • Premature Ovarian Failure 2B
    OMIM # 300604
    POF2B
  • Porphyria, Congenital Erythropoietic
    OMIM # 263700
    CEP, Gunther Disease, Uroporphyrinogen III Synthase, Deficiency of, UROS Deficiency
  • Uroporphyrinogen III Synthase
    OMIM # 606938
    UROS
  • Pituitary Adenoma 4, ACTH-Secreting
    OMIM # 219090
    PITA4, Cushing Disease, Pituitary
  • Pentosuria
    OMIM # 260800
    PNTSU, L-Xylulosuria, Xylitol Dehydrogenase Deficiency, L-Xylulose Reductase Deficiency,
  • Pendred Syndrome
    OMIM # 274600
    PDS, Deafness with Goiter, Goiter-Deafness Syndrome, Thyroid Hormonogenesis, Genetic Defect In, 2B, Hypothyroidism, Congenital, due to Dyshormonogenesis, 2B, Thyroid Hormone Organification Defect IIB
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