Macular atrophy

Symptom Information:

Symptom ID: HPO:0007401
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Macular degeneration
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)
                         Abnormality of the macula(HPO:0001103)
                            Macular degeneration(HPO:0000608)
                               Macular atrophy(HPO:0007401)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL (OMIM:601341)
Adult-onset foveomacular vitelliform dystrophy (Orphanet:99000)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 5 (OMIM:615983)
CONE-ROD DYSTROPHY 11 (OMIM:610381)
CONE-ROD DYSTROPHY 16 (OMIM:614500)
Leber congenital amaurosis 4 (OMIM:604393)
MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2 (OMIM:616171)
RETINITIS PIGMENTOSA 11 (OMIM:600138)
RETINITIS PIGMENTOSA 38 (OMIM:613862)
RETINITIS PIGMENTOSA 9 (OMIM:180104)
Retinal degeneration - nanophthalmos - glaucoma (Orphanet:1574)