An eye disease characterized by abnormalities of the front part of the eye, the anterior segment. [ url:http://en.wikipedia.org/wiki/Axenfeld_syndrome url:http://ghr.nlm.nih.gov/condition/axenfeld-rieger-syndrome http://purl.obolibrary.org/obo/ECO_0007637 http://purl.obolibrary.org/obo/ECO_0007638 ]
Synonyms: Axenfeld syndrome Rieger's anomaly Anomaly, Rieger's RGS - Rieger syndrome
Term information
- MESH:C535679
- ICD10CM:Q13.81
- UMLS_CUI:C0265341
- ORDO:782
- GARD:5701
- NCI:C131001
- MIM:PS180500
- SNOMEDCT_US_2023_03_01:47507006
DO_rare_slim, NCIthesaurus
Term relations
- autosomal dominant disease
- eye disease
- disease has location some eye
- has material basis in some autosomal dominant inheritance