About EGF-related primary hypomagnesemia with intellectual disability
EGF-related primary hypomagnesemia with intellectual disability is a rare disease catalogued by Orphanet (ORPHA:620368). It is associated with the EGF gene. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to EGF-related primary hypomagnesemia with intellectual disability trials.
Search ClinicalTrials.gov for "EGF-related primary hypomagnesemia with intellectual disability" or filter by Orphanet code ORPHA:620368 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting EGF-related primary hypomagnesemia with intellectual disability trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for EGF-related primary hypomagnesemia with intellectual disability. Updated daily.