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Lennox-Gastaut syndrome
3 associated genes
54 connected diseases
No signs/symptoms info
Disease Type of connection
Epilepsy with myoclonic-astatic seizures
Dravet syndrome
Familial or sporadic hemiplegic migraine
Generalized epilepsy with febrile seizures-plus context
Malignant migrating partial seizures of infancy
Familial pancreatic carcinoma
Precursor B-cell acute lymphoblastic leukemia
Early-onset autosomal dominant Alzheimer disease
Multiple endocrine neoplasia type 1
Kostmann syndrome
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Anaplastic ependymoma
Romano-Ward syndrome
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal recessive primary microcephaly
Familial melanoma
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Peters anomaly
Precursor T-cell acute lymphoblastic leukemia
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Alternating hemiplegia of childhood
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Autosomal dominant dopa-responsive dystonia
Bardet-Biedl syndrome
Behavioral variant of frontotemporal dementia
Cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss
Cone rod dystrophy
Familial isolated dilated cardiomyopathy
GTP cyclohydrolase I deficiency
Idiopathic CD4 lymphocytopenia
Joubert syndrome with oculorenal defect
Leber congenital amaurosis
Meckel syndrome
Progressive non-fluent aphasia
Rapid-onset dystonia-parkinsonism
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Semantic dementia
Senior-Loken syndrome
Young adult-onset Parkinsonism
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Multiple endocrine neoplasia type 4
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: C535500
Gene symbol UniProt reference OMIM reference
CHD2 O14647602119
MAPK10 P53779602897
SCN1A P35498182389
No signs/symptoms info available.