Term Name:	cataract 22 multiple types
Synonyms:	autosomal recessive congenital nuclear cataract 2, CATCN2, CTRCT22
Definition:	A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B3 crystallin gene (CRYBB3) on chromosome 22q11.
Ontology:	Human Disease [DOID:0110268]   ( DOID:0110268 )