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:0111803 - syndromic microphthalmia 8

Disease Ontology Definition:A syndromic microphthalmia characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs, prognathism and intellectual disability that has_material_basis_in mutation in a region of chromosome 6q21.

Synonyms: MCOPS8, microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome, MMEP syndrome, syndromic microphthalmia type 8, Viljoen-Smart syndrome

Xenbase Genes : snx3



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal genetic disease (is_a), syndromic microphthalmia (is_a)