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early myoclonic encephalopathy

Disease Summary
Associated Targets (24)
Tbio

12

Tclin

9

Tchem

3


Explore Associated Targets
Mondo Description Early myoclonic encephalopathy (EME) is characterized clinically by the onset of fragmentary myoclonus appearing in the first month of life, often associated with erratic focal seizures and a suppression-burst EEG pattern.
Mondo Term and Equivalent IDs
MONDO:0016022:  early myoclonic encephalopathy
EFO:1001900: 
GARD:0007142: 
NCIT:C116593: 
Orphanet:1935: 
SCTID:44423001: 
UMLS:C0014550: 
UMLS:C0270855: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)