Search Ontology:

Human Disease

Axenfeld-Rieger syndrome

Term ID

DOID:14686

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
MIM:PS180500
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 Pages

Alliance (1)

Genes Involved

Zebrafish Models