A syndrome characterized by multiple congenital anomalies, mental retardation, sensorineural deafness, talon cusps of upper central incisors, growth retardation, and bilateral symmetric digital anomalies mainly in the form of preaxial brachydactyly and hyperphalangism.

Name Development Level Target Family
Name Description
TCRDv4.6.9
JensenLab Text Mining
UniProt Disease