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GTR Home > Conditions/Phenotypes > Hyperostosis cranialis interna

Hyperostosis cranialis interna

Synonyms
Hyperostosis cranalis interna
Modes of inheritance
Autosomal dominant inheritance (Orphanet)

Summary

Hyperostosis cranialis interna (HCIN) is a bone disorder characterized by endosteal hyperostosis and osteosclerosis of the calvaria and the skull base. The progressive bone overgrowth causes entrapment and dysfunction of cranial nerves I, II, V, VII, and VIII (Waterval et al., 2010). [from OMIM]

Available tests

10 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (10 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19, SLC39A14
    Summary: solute carrier family 39 member 14

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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