About   Help   FAQ
Disease Ontology Browser
Cri-Du-Chat syndrome (DOID:12580)
Alliance: disease page
Synonyms: 5p deletion syndrome; 5p partial monosomy syndrome; chromosome 5 short arm deletion syndrome; chromosome 5p deletion syndrome
Alt IDs: OMIM:123450, ICD10CM:Q93.4, ICD9CM_2006:758.31, ICD9CM:758.31, MESH:D003410, NCI:C34518, UMLS_CUI:C0010314
Definition: 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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory