Literature record
Complete aniridia with central keratopathy and congenital glaucoma is a CYP1B1-related phenotype.
PMID 23767995 | DOI 10.3109/13816810.2013.804096 · Ophthalmic genetics · 2014 · View on PubMed ↗
Source-grounded extraction
Validated evidence
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| phenotype | primary congenital glaucoma | “Complete aniridia with central keratopathy and congenital glaucoma is a CYP1B1-related phenotype.” | 0.93 | phenotype_alias_lexicon_v2 |