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MIRAGE
holoprosencephaly 11

Summary
Synonym
  • HPE11
Definition
A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24.
Super Class
autosomal dominant disease holoprosencephaly
Disease Ontology
DOID:0110877
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
50937 CDON cell adhesion associated, oncogene regulated
Displaying 1 entry
Gene ID Gene Symbol Description Source
57810 Cdon cell adhesion molecule-related/down-regulated by oncogenes
Related Glycoprotein
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025