Variants
Sign InSign Up

46,XX disorder of sex development-anorectal anomalies syndrome

Your Results

Sign In

Description

46,XX disorder of sex development-anorectal anomalies syndrome is a rare developmental defect during embryogenesis syndrome characterized by a normal female karyotype, normal ovaries, male or ambiguous genitalia, urinary tract malformations (ranging from bilateral renal agenesis to mild unilateral hydronephrosis), Müllerian duct anomalies (e.g. complete absence of the uterus and vagina, bicornuate uterus), and imperforate anus. Additional features may include tracheoesophageal fistula, radial aplasia, and malrotation of the gut.

ORDO

  • Mode of Inheritance

    VARIANTS

    0

    Genes

      External Links

      • OMIM
      • Orphanet

        2973

      • HPO
      • Medgen

        CN203326

      © 2024 Biocodify. All rights reserved.

      TwitterTwitter

      Product

      HomePricingDashboard

      Stay up to date

      The latest news and updates from Biocodify, sent to your inbox.