U.S. flag

An official website of the United States government

GTR Home > Conditions/Phenotypes > Intellectual developmental disorder, X-linked 112

Intellectual developmental disorder, X-linked 112

Summary

X-linked intellectual disorder-112 (XLID112) is a neurodevelopmental disorder characterized by developmental delay, with speech delay more prominent than motor delay, autism or autism traits, and variable dysmorphic features. Affected females have been reported, which appears to be related to skewed X-inactivation (summary by Hiatt et al., 2023). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: DXS6673E, MYM, XFIM, XLID112, ZNF198L2, ZNF261, ZMYM3
    Summary: zinc finger MYM-type containing 3

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.