Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0060417 - 3p deletion syndrome


Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in a contiguous gene deletion syndrome involving chromosome 3pter-p25 and is characterized by low birth weight, microcephaly, trigonocephaly, hypotonia, psychomotor and growth retardation, ptosis, telecanthus, downslanting palpebral fissures, and micrognathia.

Synonyms: chromosome 3pter-P25 deletion syndrome, distal monosomy 3p

In OMIM:
OMIM:613792 - CHROMOSOME 3pter-p25 DELETION SYNDROME

In Mondo Disease Ontology:
MONDO:0013424 - 3p- syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes :

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a)