Search Ontology:
Human Disease

cataract 13 with adult i phenotype

Term ID
DOID:0110242
Synonyms
  • CTRCT13
Definition
A cataract that has_material_basis_in homozygous or compound heterozygous mutation in the GCNT2 gene on chromosome 6p24. https://www.ncbi.nlm.nih.gov/pubmed/11739194
References
Ontology
Human Disease   ( DOID:0110242 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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