Retinitis pigmentosa inversa

Symptom Information:

Symptom ID: HPO:0008035
Synonyms:
Central retinitis pigmentosa [HPO:0008035]
Central retinitis pigmentosa [OMIM:Central retinitis pigmentosa]
Retinitis pigmentosa inversa [OMIM:Retinitis pigmentosa inversa]
Quality:
Cross references:
OMIM: "Central retinitis pigmentosa" [OMIM:Central retinitis pigmentosa]
OMIM: "Retinitis pigmentosa inversa" [OMIM:Retinitis pigmentosa inversa]
Is a (Direct Parents):
HPO         Rod-cone dystrophy
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)
                            Abnormality of retinal pigmentation(HPO:0007703)
                               Rod-cone dystrophy(HPO:0000510)
                                  Retinitis pigmentosa inversa(HPO:0008035)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS (OMIM:268010)
STARGARDT DISEASE 1 (OMIM:248200)
Stargardt disease (Orphanet:827)