Abnormally prominent line of Schwalbe

Symptom Information:

Symptom ID: HPO:0007873
Synonyms:
Prominent Schwalbe lines [HPO:0007873]
Abnormally prominent line of Schwalbe [OMIM:Abnormally prominent line of Schwalbe]
Prominent Schwalbe lines [OMIM:Prominent Schwalbe lines]
Prominent Schwalbe line (posterior embryotoxon) [OMIM:Prominent Schwalbe line (posterior embryotoxon)]
Quality:
Cross references:
OMIM: "Abnormally prominent line of Schwalbe" [OMIM:Abnormally prominent line of Schwalbe]
OMIM: "Prominent Schwalbe lines" [OMIM:Prominent Schwalbe lines]
OMIM: "Prominent Schwalbe line (posterior embryotoxon)" [OMIM:Prominent Schwalbe line (posterior embryotoxon)]
Is a (Direct Parents):
HPO         Abnormality of the line of Schwalbe
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)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the cornea(HPO:0000481)
                      Abnormality of the line of Schwalbe(HPO:0008048)
                         Abnormally prominent line of Schwalbe(HPO:0007873)
MedDRA:
Database Frequency: 4 / 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, TYPE 1 (OMIM:180500)
Axenfeld-Rieger syndrome (Orphanet:782)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)