Gorlin-Chaudhry-Moss syndrome
Synonyms: Craniofacial dysostosis-genital, dental, cardiac anomalies syndrome | Cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome | Dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome | GCM syndrome
Gorlin-Chaudhry-Moss (GCM) syndrome is a multiple congenital anomaly syndrome characterized by craniofacial dysostosis facial dysmorphism conductive hearing loss generalized hypertrichosis and extremity ocular and dental anomalies.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version May 2024
Newly diagnosed with
Gorlin-Chaudhry-Moss syndrome?
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Advocacy Organizations
National Foundation for Ectodermal Dysplasias
The NFED mission is to empower and connect those touched by ectodermal dysplasias through education, support and research.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.