Term Name: | Axenfeld-Rieger syndrome type 1 |
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Synonyms: | RIEG1, Rieger syndrome type 1 |
Definition: | An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the homeobox transcription factor gene PITX2 on chromosome 4q25. |
Ontology: | Human Disease [DOID:0110120] ( DOID:0110120 ) |