EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 8
OrphanetNr:
OMIM Id: 615744
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
 (HPO:0200134) Epileptic encephalopathy 42 / 7739
2
 (HPO:0001263) Global developmental delay 853 / 7739
3
 (HPO:0002373) Febrile seizures 37 / 7739
4
 (HPO:0002133) Status epilepticus 59 / 7739
5
 (HPO:0001249) Intellectual disability 1089 / 7739
6
 (HPO:0010819) Atonic seizures 18 / 7739
7
 (HPO:0006813) Hemiclonic seizures 3 / 7739
8
 (HPO:0002121) Absence seizures 62 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: