Term Name: cataract 33
Synonyms: cortical cataract 33, CTRCT33
Definition: A cataract that has_material_basis_in homozygous mutation in the beaded filament structural protein-1 gene (BFSP1) on chromosome 20p12.
Ontology: Human Disease [DOID:0110264]   ( DOID:0110264 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease cataract