|OBO ID: DOID:0070354|
|Term Name:||cataract 48||Search Ontology:|
|Definition:||A cataract that has_material_basis homozygous mutation in the DNMBP gene on chromosome 10q24 and is characteriaed by infantile or early-childhood cataracts and visual impairment. (2)|
|Ontology:||Human Disease (DOID:0070354)|
|is a type of:||
OTHER cataract 48 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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