ODCs

Click node...

Juvenile myoclonic epilepsy

9 OMIM references -
7 associated genes
33 connected diseases
No signs/symptoms info

Disease	Type of connection
Childhood absence epilepsy
Benign familial infantile seizures
Benign familial neonatal seizures
1p36 deletion syndrome
Episodic ataxia type 5
Generalized epilepsy with febrile seizures-plus context
Juvenile absence epilepsy
Leukoencephalopathy with mild cerebellar ataxia and white matter edema
Autoimmune lymphoproliferative syndrome
Alternating hemiplegia of childhood
Benign paroxysmal torticollis of infancy
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Spinocerebellar ataxia type 6
Catecholaminergic polymorphic ventricular tachycardia
Benign familial neonatal-infantile seizures
Early infantile epileptic encephalopathy
Spinocerebellar ataxia type 14
Autosomal dominant nonsyndromic intellectual deficit
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Familial isolated dilated cardiomyopathy
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Leprechaunism
Muscular dystrophy, Selcen type
Rabson-Mendenhall syndrome
Spinocerebellar ataxia type 1
Autosomal dominant nonsyndromic sensorineural deafness type DFNA

Synonym(s): (no synonyms)

Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (ICD10): - Diseases of the nervous system -

Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: normal Type of inheritance: autosomal dominant		External references: 9 OMIM references - 1 MeSH reference: D020190

No signs/symptoms info available.