Term Name:	cataract 17 multiple types
Synonyms:	autosomal recessive congenital nuclear cataract 3, CATCN3, CTRCT17
Definition:	A cataract that has_material_basis_in heterozygous or homozygous mutation in the beta-B1 crystallin gene (CRYBB1) on chromosome 22q12.
Ontology:	Human Disease [DOID:0110270]   ( DOID:0110270 )