Macular atrophy
Symptom Information:
Symptom ID: | HPO:0007401 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |