No hippocampal sclerosis
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Direct Parents): |
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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:
Benign familial mesial temporal lobe epilepsy | (Orphanet:163717) |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 2 | (OMIM:608096) |