Rieger anomaly

Symptom Information:

Symptom ID: HPO:0000558
Synonyms:
Rieger anomaly [OMIM:Rieger anomaly]
Rieger anomaly (goniodysgenesis) [OMIM:Rieger anomaly (goniodysgenesis)]
Quality:
Cross references:
OMIM: "Rieger anomaly" [OMIM:Rieger anomaly]
OMIM: "Rieger anomaly (goniodysgenesis)" [OMIM:Rieger anomaly (goniodysgenesis)]
Is a (Direct Parents):
HPO         Hypoplasia of the iris
HPO         Anterior segment dysgenesis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Aplasia/Hypoplasia affecting the eye(HPO:0008056)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
                   Aplasia/Hypoplasia affecting the uvea(HPO:0008055)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the anterior chamber(HPO:0000593)
                      Anterior segment dysgenesis(HPO:0007700)
                         Rieger anomaly(HPO:0000558)
                   Aplasia/Hypoplasia affecting the anterior segment of the eye(HPO:0008062)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
                   Abnormality of the iris(HPO:0000525)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
                   Aplasia/Hypoplasia affecting the uvea(HPO:0008055)
                      Aplasia/Hypoplasia of the iris(HPO:0008053)
                         Hypoplasia of the iris(HPO:0007676)
                            Rieger anomaly(HPO:0000558)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES (OMIM:109120)
Axenfeld-Rieger syndrome (Orphanet:782)
GMS syndrome (Orphanet:2090)
SHORT syndrome (Orphanet:3163)
Wolf-Hirschhorn syndrome (Orphanet:280)