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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations