Retinal pigment epithelial atrophy

Symptom Information:

Symptom ID: HPO:0007722
Synonyms:
Loss of retinal pigment epithelium [OMIM:Loss of retinal pigment epithelium]
Quality:
Cross references:
OMIM: "Loss of retinal pigment epithelium" [OMIM:Loss of retinal pigment epithelium]
Is a (Direct Parents):
HPO         obsolete Abnormality of the retinal pigment epithelium
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)
                         obsolete Abnormality of the retinal pigment epithelium(HPO:0008051)
                            Retinal pigment epithelial atrophy(HPO:0007722)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Chorioretinopathy, Birdshot type (Orphanet:179)
Microphthalmia - retinitis pigmentosa - foveoschisis - optic disc drusen (Orphanet:251279)
RETINITIS PIGMENTOSA 19 (OMIM:601718)
RETINITIS PIGMENTOSA 31 (OMIM:609923)
RETINITIS PIGMENTOSA 33 (OMIM:610359)
RETINITIS PIGMENTOSA 44 (OMIM:613769)
Retinal macular dystrophy type 2 (Orphanet:319640)
Retinopathy, Burgess-Black type (Orphanet:139455)
Wagner disease (Orphanet:898)