Secondary generalization

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Secondary generalization (rare) [OMIM:Secondary generalization (rare)]
Quality:
Cross references:
OMIM: "Secondary generalization" [OMIM:Secondary generalization]
OMIM: "Secondary generalization (rare)" [OMIM:Secondary generalization (rare)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

EPILEPSY, FAMILIAL TEMPORAL LOBE, 4 (OMIM:611631)
Familial focal epilepsy with variable foci (Orphanet:98820)
Progressive myoclonic epilepsy type 3 (Orphanet:263516)