Intractable seizures

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Seizures, intractable [OMIM:Seizures, intractable]
Seizures, intractable (1 family) [OMIM:Seizures, intractable (1 family)]
Quality:
Cross references:
OMIM: "Intractable seizures" [OMIM:Intractable seizures]
OMIM: "Seizures, intractable" [OMIM:Seizures, intractable]
OMIM: "Seizures, intractable (1 family)" [OMIM:Seizures, intractable (1 family)]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 12 / 7739
Resource:

All diseases associated with this symptom:

Alpers syndrome (Orphanet:726)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17 (OMIM:615473)
Early infantile epileptic encephalopathy without suppression burst (Orphanet:369894)
Guanidinoacetate methyltransferase deficiency (Orphanet:382)
Infantile epileptic-dyskinetic encephalopathy (Orphanet:364063)
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 (OMIM:615228)
Methylmalonic acidemia with homocystinuria, type cblX (Orphanet:369962)
Phosphoserine aminotransferase deficiency (Orphanet:284417)
Spasticity - intellectual deficit - X-linked epilepsy (Orphanet:3175)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)