Search Ontology:
Human Disease

cataract 48

Term ID
DOID:0070354
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. (2)
References
Ontology
Human Disease   ( DOID:0070354 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models