About   Help   FAQ
Disease Ontology Browser
Wolf-Hirschhorn syndrome (DOID:0050460)
Alliance: disease page
Synonyms: 4p deletion syndrome; chromosome 4p16.3 deletion syndrome; PITT SYNDROME; Pitt-Rogers-Danks Syndrome
Alt IDs: OMIM:194190, DOID:6684, ICD10CM:Q93.3, MESH:D054877, NCI:C35528, ORDO:280, UMLS_CUI:C0796117, UMLS_CUI:C1956097
Definition: A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3.

Disease References using Mouse Models (4)
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
03/18/2025
MGI 6.24 		The Jackson Laboratory