OBO ID: DOID:0110242 |
Term Name: | cataract 13 with adult i phenotype | Search Ontology: | |
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Synonyms: |
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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: |
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Ontology: | Human Disease ( DOID:0110242 ) |
OTHER cataract 13 with adult i phenotype PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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GCNT2 | Cataract 13 with adult i phenotype |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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