Variants
Sign InSign Up

Holoprosencephaly 9

Your Results

Sign In

Description

Holoprosencephaly-9 refers to a disorder characterized by a wide phenotypic spectrum of brain developmental defects, with or without overt forebrain cleavage abnormalities. It usually includes midline craniofacial anomalies involving the first branchial arch and/or orbits, pituitary hypoplasia with panhypopituitarism, and postaxial polydactyly. The disorder shows incomplete penetrance and variable expressivity (summary by Roessler et al., 2003 and Bertolacini et al., 2012). For general phenotypic information and a discussion of genetic heterogeneity of holoprosencephaly, see HPE1 (236100).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance
  • Sporadic

VARIANTS

207

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    610829

  • Orphanet
  • HPO
  • Medgen

    C1835819

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

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