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Summary Literature (0)
DOID:0110242 - cataract 13 with adult i phenotype

Disease Ontology Definition:A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24.

Synonyms: CTRCT13

Xenbase Genes : gcnt2.2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007289 - presumptive rhombomere 1


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)