Disease Browser
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Parent Node: epilepsy syndrome (MONDO:0015650) | ..Starting node ..epileptic encephalopathy, infantile or early childhood ()
| Child Nodes:
| ........epileptic encephalopathy, infantile or early childhood, 1 () | ........epileptic encephalopathy, infantile or early childhood, 2 () | ........epileptic encephalopathy, infantile or early childhood, 3 () |
Sister Nodes: | ..adolescent-onset epilepsy syndrome ()
| ..adolescent/adult-onset epilepsy syndrome ()
| ..atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome ()
| ..childhood-onset epilepsy syndrome ()
| ..cortical dysplasia-focal epilepsy syndrome ()
| ..DEND syndrome ()
| ..epilepsy-telangiectasia syndrome ()
| ..epileptic encephalopathy, infantile or early childhood ()
| ..infantile epilepsy syndrome ()
| ..Moynahan syndrome ()
| ..neonatal epilepsy syndrome ()
| ..neonatal/infantile epilepsy syndrome ()
| ..oculocerebrocutaneous syndrome ()
| ..Pallister-W syndrome ()
| ..PEHO syndrome ()
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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: | 20627 |
Name: | epileptic encephalopathy, infantile or early childhood |
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Reference: |
MedGen:
MeSH:
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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