Variants
Sign InSign Up

Seckel syndrome 5

Your Results

Sign In

Description

Seckel syndrome is an autosomal recessive disorder characterized by proportionate short stature, severe microcephaly, mental retardation, and a typical 'bird-head' facial appearance (summary by Kalay et al., 2011). For a general phenotypic description and a discussion of genetic heterogeneity of Seckel syndrome, see 210600.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

106

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    613823

  • Orphanet
  • HPO
  • Medgen

    C3151187

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard