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FOXE3 and primary congenital glaucoma are reported together in 1 article.
Gene
FOXE3
- HGNC
- HGNC:3808
4articles
4mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Primary congenital glaucoma
70articles
70mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
1 records shown · first 60Molecular basis of Peters anomaly in Saudi Arabia.
PMID 15621878 | DOI 10.1080/13816810490902648 · Ophthalmic genetics · 2004 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | FOXE3 | “The coding exons of FOXC1, PITX2, and PAX6 were screened and those of CYP1B1 and FOXE3 sequenced.” | 0.98 | hgnc_dict_v1 |
| phenotype | primary congenital glaucoma | “Peters anomaly (PA) and primary congenital glaucoma (PCG) are genetically and phenotypically distinct conditions.” | 0.98 | phenotype_alias_lexicon_v2 |
| gene | CYP1B1 | “Mutations in cytochrome P4501B1 (CYP1B1) are the most common cause of PCG in Saudi Arabia.” | 0.98 | hgnc_dict_v1 |
| gene | FOXC1 | “The coding exons of FOXC1, PITX2, and PAX6 were screened and those of CYP1B1 and FOXE3 sequenced.” | 0.98 | hgnc_dict_v1 |