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 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 Monosomy 5p