Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0050460 - Wolf-Hirschhorn syndrome

Disease Ontology 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.

Synonyms: 4p deletion syndrome, PITT SYNDROME, Pitt-Rogers-Danks Syndrome, chromosome 4p16.3 deletion syndrome,

Echinobase Genes : fgfrl1, letm1


OMIM:
MIM:194190 - wolf-hirschhorn syndrome; whs

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): chromosomal deletion syndrome (is_a)