Disease Directory Growth delay-intellectual disability-hepatopathy syndrome
Rare Disease

Growth delay-intellectual disability-hepatopathy syndrome

Type

Disease

Gene

IARS1

About Growth delay-intellectual disability-hepatopathy syndrome

Growth delay-intellectual disability-hepatopathy syndrome is a rare disease catalogued by Orphanet (ORPHA:541423). It is associated with the IARS1 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 Growth delay-intellectual disability-hepatopathy syndrome trials.

Search ClinicalTrials.gov for "Growth delay-intellectual disability-hepatopathy syndrome" or filter by Orphanet code ORPHA:541423 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

Patient Organization

Orphanet

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Orphanet

European reference resource for rare diseases (ORPHA:541423)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Growth delay-intellectual disability-hepatopathy syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Growth delay-intellectual disability-hepatopathy syndrome. Updated daily.