Search Ontology:
Human Disease

cataract 18

Term ID
DOID:0110238
Synonyms
  • autosomal recessive congenital cataract 2
  • cataract 18 autosomal recessive
  • CATC2
  • CTRCT18
Definition
A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3. https://www.ncbi.nlm.nih.gov/pubmed/21636066
References
Ontology
Human Disease   ( DOID:0110238 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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