Term Name: cataract 41
Synonyms: congenital nuclear type cataract 41, CTRCT41
Definition: A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.
Ontology: Human Disease [DOID:0110241]   ( DOID:0110241 )

Relationships
is a type of: autosomal dominant disease cataract