Variants
Sign InSign Up

Terminal osseous dysplasia-pigmentary defects syndrome

Your Results

Sign In

Description

Terminal osseous dysplasia is an X-linked dominant male-lethal disease characterized by skeletal dysplasia of the limbs, pigmentary defects of the skin, and recurrent digital fibroma during infancy (Sun et al., 2010).

OMIM

  • Mode of Inheritance

  • X-linked dominant inheritance

VARIANTS

15

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    300244

  • Orphanet

    88630

  • HPO
  • Medgen

    C1846129

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard