Term Name:	chromosome 19q13.11 deletion syndrome
Synonyms:	19q13.11 microdeletion syndrome, monosomy 19q13.11
Definition:	A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties.
Ontology:	Human Disease [DOID:0060408]   ( DOID:0060408 )