U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Brachydactyly type A1D

Summary

Any brachydactyly type A1 in which the cause of the disease is a mutation in the BMPR1B gene. [from MONDO]

Available tests

18 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: ALK-6, ALK6, AMD3, AMDD, BDA1D, BDA2, CDw293, BMPR1B
    Summary: bone morphogenetic protein receptor type 1B

Clinical features

Help

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.