Term Name:	chromosome 16q22 deletion syndrome
Synonyms:
Definition:	A chromosomal deletion syndrome that has_material_basis_in an interstitial 16q22 deletion that is characterized by a failure to thrive in infancy, poor growth, delayed psychomotor development, hypotonia, and dysmorphic features, including large anterior fontanel, high forehead, diastasis of the cranial sutures, broad nasal bridge, hypertelorism, low-set abnormal ears, and short neck.
Ontology:	Human Disease [DOID:0060401]   ( DOID:0060401 )