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DOID:0110263 - cataract 19 multiple types
Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the LIM2 gene on chromosome 19q13.
Synonyms: CTRCT19
Xenbase Genes

MONDO:0014111 - cataract 19 multiple types |
MIM:615277 - CATARACT 19, MULTIPLE TYPES; CTRCT19 |
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)