Peters anomaly

Symptom Information:

Symptom ID: HPO:0000659
Synonyms:
Peters anomaly [OMIM:Peters anomaly]
Peter's anomaly [OMIM:Peter's anomaly]
Peter's anomaly (congenital anomaly of the anterior segment) [OMIM:Peter's anomaly (congenital anomaly of the anterior segment)]
Peters anomaly (WWS) [OMIM:Peters anomaly (WWS)]
Peters anomaly (rare) [OMIM:Peters anomaly (rare)]
Quality:
Cross references:
OMIM: "Peters anomaly" [OMIM:Peters anomaly]
OMIM: "Peter's anomaly" [OMIM:Peter's anomaly]
OMIM: "Peter's anomaly (congenital anomaly of the anterior segment)" [OMIM:Peter's anomaly (congenital anomaly of the anterior segment)]
OMIM: "Peters anomaly (WWS)" [OMIM:Peters anomaly (WWS)]
OMIM: "Peters anomaly (rare)" [OMIM:Peters anomaly (rare)]
Is a (Direct Parents):
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)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the anterior chamber(HPO:0000593)
                      Anterior segment dysgenesis(HPO:0007700)
                         Peters anomaly(HPO:0000659)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

17q12 microduplication syndrome (Orphanet:261272)
Histiocytoid cardiomyopathy (Orphanet:137675)
Isolated aniridia (Orphanet:250923)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 (OMIM:613150)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
Muscle-eye-brain disease (Orphanet:588)
Peters anomaly (Orphanet:708)
Peters-plus syndrome (Orphanet:709)
Subaortic stenosis - short stature (Orphanet:3191)