disease has feature Strabismus syndromic disease Cri-du-chat syndrome https://github.com/monarch-initiative/mondo/issues/6744 https://www.malacards.org/card/cri_du_chat_syndrome icd11.foundation:620584190 deletion 5p 5p- syndrome Orphanet:281 DECIPHER:2 Cri du Chat Syndrome This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'disorder of visual system' (MONDO:0024458) ontology branch (https://orcid.org/0000-0001-9310-0163) Cat-Cry syndrome MEDGEN:41345 NORD:1015 Cri-du-chat syndrome 5p deletion syndrome 5p partial monosomy syndrome SCTID:70173007 NANDO:2200961 MONDO:0007404 chromosome 5p- syndrome 5p minus syndrome MESH:D003410 Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism. NANDO:1200684 monosomy type 5p UMLS:C0010314 GARD:0006213 DOID:12580 OMIM:123450 MedDRA:10011385 ICD9:758.39 Cri du chat syndrome NCIT:C34518 chromosome 5p deletion syndrome ICD9:758.31 partial deletion of the short arm of chromosome 5 obsolete chromosomal anomaly with cataract