Variants
Genes
Phenotypes
Pricing
Sign InSign Up

Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome

Your Results

Sign In

Description

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

2

SEE THE VARIANTS →

Genes

  • CTBP1

External Links

  • OMIM

    617915

  • Orphanet
  • HPO
  • Medgen

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

DNA

VariantsGenesPhenotypes

Stay up to date

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