Term Name:	cataract 48
Synonyms:	CTRCT48
Definition:	A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment.
Ontology:	Human Disease [DOID:0070354]   ( DOID:0070354 )