Disease Browser
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Parent Node: infantile epilepsy syndrome (MONDO:0020071) | Parent Node: neonatal epilepsy syndrome (MONDO:0020070) | ..Starting node ..undetermined early-onset epileptic encephalopathy ()
| Child Nodes:
| ........epileptic encephalopathy, early infantile, 13 () | ........epileptic encephalopathy, early infantile, 21 () | ........epileptic encephalopathy, early infantile, 24 () | ........epileptic encephalopathy, early infantile, 25 () | ........epileptic encephalopathy, early infantile, 26 () | ........epileptic encephalopathy, early infantile, 28 () | ........epileptic encephalopathy, early infantile, 29 () | ........epileptic encephalopathy, early infantile, 31 () | ........epileptic encephalopathy, early infantile, 32 () | ........epileptic encephalopathy, early infantile, 33 () | ........epileptic encephalopathy, early infantile, 41 () | ........epileptic encephalopathy, early infantile, 42 () | ........epileptic encephalopathy, early infantile, 44 () | ........epileptic encephalopathy, early infantile, 45 () | ........epileptic encephalopathy, early infantile, 46 () | ........epileptic encephalopathy, early infantile, 47 () |
Sister Nodes: | ..benign idiopathic neonatal seizures ()
| ..benign neonatal seizures ()
| ..epileptic encephalopathy with global cerebral demyelination () L: 00107;
| ..malignant migrating partial seizures of infancy ()
| ..severe neonatal-onset encephalopathy with microcephaly ()
| ..undetermined early-onset epileptic encephalopathy ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 18614 |
Name: | undetermined early-onset epileptic encephalopathy |
Definition: | |
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Synonyms: | undetermined EOEE |
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Reference: |
MedGen:
MeSH:
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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