Preferred Label : Frank-ter Haar syndrome;
ICD-11 definition : Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles
syndrome) is defined by the association of megalocornea, multiple skeletal anomalies,
characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism,
prominent eyes, full cheeks and micrognathia) and developmental delay.;
ICD-11 synonym : Ter Haar syndrome;
Origin ID : 1643548765;
Automatic exact mappings (from CISMeF team)
Frank-ter Haar syndrome (formerly considered as an autosomal recessive form of Melnick-Needles
syndrome) is defined by the association of megalocornea, multiple skeletal anomalies,
characteristic facial dysmorphism (wide fontanels, prominent forehead, hypertelorism,
prominent eyes, full cheeks and micrognathia) and developmental delay.
