Search Ontology:
Human Disease

cataract 41

Term ID
DOID:0110241
Synonyms
  • congenital nuclear type cataract 41
  • CTRCT41
Definition
A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16. https://www.ncbi.nlm.nih.gov/pubmed/23531866
References
Ontology
Human Disease   ( DOID:0110241 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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