chromosomal deletion syndrome Cri-Du-Chat syndrome GARD:6213 OMIM mapping confirmed by DO. [SN]. A syndrome that has_material_basis_in deletion of the end of the chromosome 5 p arm and that is characterized by intellectual disability, delayed development, small head size, low birth weight, weak muscle tone widely set eyes, low-set ears, a small jaw, a rounded face and a high-pitched cry that sounds like that of a cat. NCI:C34518 DOID:12580 ICD10CM:Q93.4 OMIM:123450 ICD9CM:758.31 5p deletion syndrome disease_ontology UMLS_CUI:C0010314 5p partial monosomy syndrome SNOMEDCT_US_2020_03_01:70173007 MESH:D003410 Cri-du-chat syndrome chromosome 5 short arm deletion syndrome chromosome 5p deletion syndrome syndrome