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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)
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03/25/2025
MGI 6.24 		The Jackson Laboratory