Phthisis bulbi
Symptom Information:
Symptom ID: | HPO:0000667 | ||
Synonyms: |
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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) Phthisis bulbi(HPO:0000667) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
Knobloch syndrome | (Orphanet:1571) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Osteoporosis - pseudoglioma | (Orphanet:2788) |