Neuronal migration defect
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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| Database Frequency: | 4 / 7739 | |
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All diseases associated with this symptom:
| Bilateral frontal polymicrogyria | (Orphanet:208444) |
| Cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation | (Orphanet:300570) |
| Polymicrogyria due to TUBB2B mutation | (Orphanet:300573) |
| X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |