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Summary Literature (0)
MIM:616994 - CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME 2; CFSMR2

Xenbase Genes:

Human Disease Resource: MIM


Disease Ontology (DO):
DOID:0081125 - craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2