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Malignant migrating partial seizures of infancy
3 OMIM references -
5 associated genes
34 connected diseases
No signs/symptoms info
Disease Type of connection
Early infantile epileptic encephalopathy
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal recessive deafness-onychodystrophy syndrome
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Dravet syndrome
Early myoclonic encephalopathy
Epilepsy with myoclonic-astatic seizures
Familial infantile myoclonic epilepsy
Familial or sporadic hemiplegic migraine
Focal epilepsy - intellectual deficit - cerebro-cerebellar malformation
Generalized epilepsy with febrile seizures-plus context
Lennox-Gastaut syndrome
Progressive myoclonic epilepsy with dystonia
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Familial multiple nevi flammei
Sturge-Weber syndrome
CLN3 disease
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Romano-Ward syndrome
Autosomal dominant hypocalcemia
Behavioral variant of frontotemporal dementia
CLN5 disease
Early-onset autosomal dominant Alzheimer disease
Familial hypocalciuric hypercalcemia type 2
Familial isolated dilated cardiomyopathy
Hereditary cerebral cavernous malformation
Progressive non-fluent aphasia
Pseudohypoaldosteronism type 2E
Semantic dementia
Young adult-onset Parkinsonism
Autoimmune lymphoproliferative syndrome
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Distal 22q11.2 microdeletion syndrome
- Malignant migrating partial epilepsy of infancy
- Migrating partial epilepsy of infancy
- Migrating partial seizures of infancy

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.