Search Ontology:
Human Disease

cataract 47

Term ID
DOID:0070353
Synonyms
  • CTRCT47
Definition
A cataract that has_material_basis_in heterozygous mutation in the SLC16A12 gene on chromosome 10q23, characterized by progressive juvenile cataract with microcornea. https://www.omim.org/entry/612018
References
Ontology
Human Disease   ( DOID:0070353 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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