axenfeld-rieger syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment. (Human Disease Ontology, DOID_14686)
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Genes

2 genes involed in the disease axenfeld-rieger syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
FOXC1 forkhead box C1
PITX2 paired-like homeodomain 2