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GTR Home > Conditions/Phenotypes > Trigonocephaly 2

Trigonocephaly 2

Summary

Trigonocephaly occurs predominantly as a nonsyndromic craniosynostosis and has an estimated prevalence of between 1:15,000 and 1:68,000 live births (summary by Vissers et al., 2011). For a discussion of genetic heterogeneity of isolated trigonocephaly, see TRIGNO1 (190440). A syndromic form of trigonocephaly is associated with monosomy for an 8-Mb interval of chromosome 9p22.3 (see 158170). [from OMIM]

Available tests

30 tests are in the database for this condition.

Clinical tests (30 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: BNAR, C9orf143, C9orf145, C9orf154, MOTA, TILRR, TRIGNO2, FREM1
    Summary: FRAS1 related extracellular matrix 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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