ZFIN Human Disease: Axenfeld-Rieger syndrome

OBO ID: DOID:14686

Term Name:	Axenfeld-Rieger syndrome		Search Ontology:
Synonyms:	Anomaly, Rieger's Axenfeld syndrome Hagedoom syndrome RGS - Rieger syndrome Rieger's anomaly
Definition:	An eye disease characterized by abnormalities of the front part of the eye, the anterior segment. (2)
References:	GARD:5701 ICD10CM:Q13.81 MESH:C535679 NCI:C131001 ORDO:782 SNOMEDCT_US_2023_03_01:47507006 UMLS_CUI:C0265341
Ontology:	Human Disease ( DOID:14686 )

Relationships

is a type of:	autosomal dominant disease eye disease autosomal dominant disease eye disease Show first 5 Terms
has subtype:	Axenfeld-Rieger syndrome type 1 Axenfeld-Rieger syndrome type 2 Axenfeld-Rieger syndrome type 3 Axenfeld-Rieger syndrome type 1 Axenfeld-Rieger syndrome type 2 Axenfeld-Rieger syndrome type 3 Show first 5 Terms

OTHER Axenfeld-Rieger syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
pitx2^mw709/mw709	standard conditions	Hendee et al., 2018
pitx2^sny6/sny6 (AB/TU)	standard conditions	Ji et al., 2016
pitx2^sny7/sny7 (AB/TU)	standard conditions	Ji et al., 2016
WT + MO6-pitx2	standard conditions	Bohnsack et al., 2012
foxc1a^nju18/nju18; f1Tg	standard conditions	Zhang et al., 2020
foxc1a^mw711/mw711; foxc1b^mw713/mw713	standard conditions	Ferre-Fernández et al., 2020

PHENOTYPE No data available

CITATIONS (7)