POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL
General Information (adopted from Orphanet):
| Synonyms, Signs: |
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| Number of Symptoms | 6 |
| OrphanetNr: | |
| OMIM Id: |
612691
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| ICD-10: |
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| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
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| Age of onset: |
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Disease classification (adopted from Orphanet):
| Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0002367) | Visual hallucinations | 8 / 7739 | ||||
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(HPO:0002133) | Status epilepticus | 59 / 7739 | ||||
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(HPO:0000718) | Aggressive behavior | 109 / 7739 | ||||
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(HPO:0002384) | Focal seizures with impairment of consciousness or awareness | 17 / 7739 | ||||
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(HPO:0002119) | Ventriculomegaly | 253 / 7739 | ||||
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(HPO:0002126) | Polymicrogyria | 64 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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