chromosome 19q13.11 deletion syndrome (DOID:0060408)
Alliance: disease page
Synonyms: 19q13.11 microdeletion syndrome; monosomy 19q13.11
Alt IDs: OMIM:613026, MESH:C567810, ORDO:217346, UMLS_CUI:C2751651
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.