U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Autosomal dominant hypocalcemia 2

Autosomal dominant hypocalcemia 2

Summary

An autosomal dominant hypocalcemia disease that has material basis in heterozygous mutation in the GNA11 gene on chromosome 19p13. [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: FBH, FBH2, FHH2, GNA-11, HG1K, HHC2, HYPOC2, GNA11
    Summary: G protein subunit alpha 11

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

Show allHide all

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.