Preferred Label : Marshall syndrome;
ICD-11 definition : Marshall syndrome is a multisystem autosomal dominant disease characterized by ocular
abnormalities, sensorineural hearing loss, craniofacial anomalies and anhidrotic ectodermal
dysplasia.;
Origin ID : 1401051186;
Automatic exact mappings (from CISMeF team)
Marshall syndrome is a multisystem autosomal dominant disease characterized by ocular
abnormalities, sensorineural hearing loss, craniofacial anomalies and anhidrotic ectodermal
dysplasia.