Term Name: Axenfeld-Rieger syndrome type 3
Synonyms: anterior chamber cleavage syndrome, anterior segment mesenchymal dysgenesis, Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss, RIEG3, Rieger syndrome type 3
Definition: An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the FOXC1 gene on chromosome 6p25.
Ontology: Human Disease [DOID:0110122]   ( DOID:0110122 )

Relationships
is a type of: Axenfeld-Rieger syndrome