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Childhood absence epilepsy
4 OMIM references -
6 associated genes
27 connected diseases
No signs/symptoms info
Disease Type of connection
Juvenile myoclonic epilepsy
Dravet syndrome
Encephalopathy due to GLUT1 deficiency
Epilepsy with myoclonic-astatic seizures
Generalized epilepsy with febrile seizures-plus context
Hereditary cryohydrocytosis with reduced stomatin
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
Paroxysmal exertion-induced dyskinesia
Spinocerebellar ataxia type 14
Autosomal dominant cervical dystonia
Benign essential blepharospasm
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Autoimmune lymphoproliferative syndrome
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Chuvash erythrocytosis
Von Hippel-Lindau disease
Periventricular nodular heterotopia
Familial isolated dilated cardiomyopathy
Muscular dystrophy, Selcen type
Generalized epilepsy - paroxysmal dyskinesia
Synonym(s):
- Pyknolepsy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.