Pericentral pigmentary retinopathy

Symptom Information:

Symptom ID: HPO:0007852
Synonyms:
Pericentral pigmentary retinopathy [OMIM:Pericentral pigmentary retinopathy]
Quality:
Cross references:
OMIM: "Pericentral pigmentary retinopathy" [OMIM:Pericentral pigmentary retinopathy]
Is a (Direct Parents):
HPO         Pigmentary retinopathy
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 posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the retina(HPO:0000479)
                         Pigmentary retinopathy(HPO:0000580)
                            Pericentral pigmentary retinopathy(HPO:0007852)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE (OMIM:268060)