U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Oculodentodigital dysplasia, autosomal recessive

Oculodentodigital dysplasia, autosomal recessive

Synonyms
OCULODENTOOSSEOUS DYSPLASIA, AUTOSOMAL RECESSIVE; ODDD, AUTOSOMAL RECESSIVE; ODOD, AUTOSOMAL RECESSIVE

Summary

Autosomal recessive form of oculodentodigital dysplasia. [from MONDO]

Available tests

41 tests are in the database for this condition.

Clinical tests (41 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: AVSD3, CMDR, CX43, EKVP, EKVP3, GJAL, HLHS1, HSS, ODDD, PPKCA, GJA1
    Summary: gap junction protein alpha 1

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.