Retinal atrophy

Symptom Information:

Symptom ID: HPO:0001105
Synonyms:
Retinal atrophy [OMIM:Retinal atrophy]
Quality:
Cross references:
OMIM: "Retinal atrophy" [OMIM:Retinal atrophy]
Is a (Direct Parents):
HPO         Abnormality of the retina
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)
                         Retinal atrophy(HPO:0001105)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

CLN10 disease (Orphanet:228337)
Congenital neuronal ceroid lipofuscinosis (Orphanet:168486)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
Muscle-eye-brain disease (Orphanet:588)
PORETTI-BOLTSHAUSER SYNDROME (OMIM:615960)
RETINITIS PIGMENTOSA 68 (OMIM:615725)
RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT (OMIM:180210)
Retinitis pigmentosa 10 (OMIM:180105)
X-linked retinoschisis (Orphanet:792)