U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Pitt-Hopkins-like syndrome 2

Pitt-Hopkins-like syndrome 2

Summary

Any Pitt-Hopkins-like syndrome in which the cause of the disease is a mutation in the NRXN1 gene. [from MONDO]

Available tests

45 tests are in the database for this condition.

Clinical tests (45 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: Hs.22998, PTHSL2, SCZD17, NRXN1
    Summary: neurexin 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.