Variants
Sign InSign Up

3p25.3 microdeletion syndrome

Your Results

Sign In

Description

3p25.3 microdeletion syndrome is a rare chromosomal anomaly characterized by intellectual disability, epilepsy or EEG abnormalities, poor speech, ataxia, and stereotypic hand movements.

ORDO

  • Mode of Inheritance

    VARIANTS

    0

    Genes

      External Links

      • OMIM
      • Orphanet

        435638

      • HPO
      • Medgen

        CN237571

      © 2024 Biocodify. All rights reserved.

      TwitterTwitter

      Product

      HomePricingDashboard

      Stay up to date

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