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GTR Home > Conditions/Phenotypes > Holoprosencephaly 11

Holoprosencephaly 11

Summary

Any holoprosencephaly in which the cause of the disease is a mutation in the CDON gene. [from MONDO]

Available tests

23 tests are in the database for this condition.

Clinical tests (23 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CDO, CDON1, HPE11, Ihog, ORCAM, CDON
    Summary: cell adhesion associated, oncogene regulated

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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