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:0110243 - cataract 46 juvenile-onset

Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the LEMD2 gene on chromosome 6p21.

Synonyms: CTRCT46, juvenilae cataract Hutterite type

Xenbase Genes : gcnt2.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008925 - cataract 46 juvenile-onset


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), cataract (is_a)