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There is a page named "SRD5A3-CDG" on Wikipedia

  • Thumbnail for SRD5A3-CDG
    SRD5A3-CDG (also known as CDG syndrome type Iq, CDG-Iq, CDG1Q or Congenital disorder of glycosylation type 1q) is a rare, non X-linked congenital disorder...
    11 KB (1,321 words) - 05:05, 1 December 2023
  • Thumbnail for SRD5A3
    an enzyme that in humans is encoded by the SRD5A3 gene. It is one of three forms of 5α-reductase. SRD5A3-CDG Congenital disorder of glycosylation Kahrizi...
    2 KB (314 words) - 05:45, 17 June 2024
  • common finding. Some CDG subtypes, like SSR4-CDG 1y, have been classified as connective tissue disorders. Ocular abnormalities of PMM2-CDG include: myopia...
    41 KB (3,740 words) - 23:31, 13 August 2024
  • Thumbnail for SLC35A1-CDG
    transport function. SRD5A3-CDG PMM2 deficiency "SLC35A1-CDG (CDG-IIf)". RESERVADOS, INSERM US14-- TODOS LOS DERECHOS. "Orphanet: SLC35A1 CDG". www.orpha.net...
    14 KB (1,432 words) - 15:08, 27 October 2023