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Cri-du-chat syndrome

Disease Summary
Associated Targets (3)
Tbio

2

Tchem

1


GARD Rare
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0007404:  Cri-du-chat syndrome
GARD:0006213: 
ICD9:758.31: 
MESH:D003410: 
NCIT:C34518: 
Orphanet:281: 
SCTID:70173007: 
UMLS:C0010314: 
UMLS:CN776901: