| Dataset | ClinVar Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Axenfeld's anomaly is a bilateral disorder characterized by a prominent, anteriorly displaced Schwalbe's line (posterior embryotoxon) and peripheral iris strands which span the anterior chamber angle to attach to Schwalbe's line. (Human Phenotype Ontology, HP_0001492) |
| External Link | http://www.ncbi.nlm.nih.gov/medgen/?term=C0266548 |
| Similar Terms | |
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1 genes associated with the Axenfeld anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| FOXC1 | forkhead box C1 |
