Contralateral hemianopsia (1 family)
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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| Is a (Whole tree): |
HPO:
MedDRA: |
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| Database Frequency: | 2 / 7739 | |
| Resource: |
All diseases associated with this symptom:
| Bilateral frontal polymicrogyria | (Orphanet:208444) |
| Polymicrogyria due to TUBB2B mutation | (Orphanet:300573) |