Disease Browser
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Parent Node: migraine disorder (MONDO:0005277) | ..Starting node ..migraine with aura ()
| Child Nodes:
| ........hemiplegic migraine () | ........migraine with aura, susceptibility to, 7 () | ........migraine with aura, susceptibility to, 9 () | ........migraine with brainstem aura () |
Sister Nodes: | ..MGR12 ()
| ..migraine with aura ()
| ..migraine with or without aura, susceptibility to, 1 ()
| ..migraine with or without aura, susceptibility to, 10 ()
| ..migraine with or without aura, susceptibility to, 11 ()
| ..migraine with or without aura, susceptibility to, 3 ()
| ..migraine with or without aura, susceptibility to, 5 ()
| ..migraine with or without aura, susceptibility to, 8 ()
| ..migraine without aura ()
| ..migraine, familial hemiplegic, 1 ()
| ..migraine, with or without aura, susceptibility to, 13 ()
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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: | 5475 |
Name: | migraine with aura |
Definition: | A migraine disorder characterized by episodes that are preceded by focal neurological symptoms. |
Alternative IDs: | |
ParentIDs: | |
TreeNumbers: | |
Synonyms: | classic migraine |
Slim Mappings: | |
Reference: |
MedGen:
MeSH:
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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