Variants
Sign InSign Up

3q26 microduplication syndrome

Your Results

Sign In

Description

A rare chromosomal anomaly with characteristics of prenatal and postnatal growth retardation, developmental delay, intellectual impairment, dysmorphic signs and variable combination of congenital anomalies, including cardiovascular, genitourinary and skeletal anomalies and spectrum of caudal malformations.

SNOMEDCT_US

  • Mode of Inheritance

    VARIANTS

    0

    Genes

      External Links

      • OMIM
      • Orphanet

        96095

      • HPO
      • Medgen

        C4755319

      © 2024 Biocodify. All rights reserved.

      TwitterTwitter

      Product

      HomePricingDashboard

      Stay up to date

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