chromosome 14q11-q22 deletion syndrome (DOID:0060392)
Alliance: disease page
Synonyms: 14q11.2 microdeletion syndrome
Alt IDs: OMIM:613457, ORDO:261120
Definition: A chromosomal deletion syndrome that is characterized by microcephaly, dysmorphic facies, psychomotor delay and failure to thrive, has_material_basis_in isolated cases of partial deletion of the long arm of chromosome 14.