|
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,
Echinobase Genes :
MIM:212500 - cataract, congenital or juvenile cataract, juvenile, hutterite type, included |
Other Model Organisms: AGR, 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)