Rare secondary generalization

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Rare secondary generalization" [OMIM:Rare secondary generalization]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Benign familial mesial temporal lobe epilepsy (Orphanet:163717)