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GTR Home > Conditions/Phenotypes > Neurodevelopmental disorder with epilepsy and hemochromatosis

Summary

Neurodevelopmental disorder with epilepsy and hemochromatosis (NEDEPH) is an X-linked recessive disorder characterized by global developmental delay, early-onset seizures, and progressive systemic iron deposition particularly affecting the liver and resulting in juvenile-onset hemochromatosis. Variable additional features may include joint contractures, visual or hearing impairment, and skin abnormalities (summary by Swoboda et al., 2014 and Muckenthaler et al., 2022). [from OMIM]

Available tests

6 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: GPI3, MCAHS2, NEDEPH, PIG-A, PNH1, PIGA
    Summary: phosphatidylinositol glycan anchor biosynthesis class A

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