Disease Browser
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Parent Node: familial focal epilepsy with variable foci (MONDO:0020310) | ..Starting node ..epilepsy, familial focal, with variable foci ()
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| ........epilepsy, familial focal, with variable foci 1 () | ........epilepsy, familial focal, with variable foci 2 () | ........epilepsy, familial focal, with variable foci 3 () | ........epilepsy, familial focal, with variable foci 4 () |
Sister Nodes: | ..epilepsy, familial focal, with variable foci ()
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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: | 215 |
Name: | epilepsy, familial focal, with variable foci |
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Synonyms: | epilepsy, familial focal, with variable foci; FFEVF |
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Reference: |
MedGen:
MeSH:
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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