Migraine with aura
Symptom Information:
Symptom ID: | HPO:0002077 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Headache(HPO:0002315) Migraine(HPO:0002076) Migraine with aura(HPO:0002077) MedDRA: Nervous system disorders(MedDRA:10029205) Headache(HPO:0002315) Migraine(HPO:0002076) Migraine with aura(HPO:0002077) |
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Database Frequency: | 14 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CADASIL | (Orphanet:136) |
EPILEPSY, FAMILIAL TEMPORAL LOBE, 4 | (OMIM:611631) |
Familial or sporadic hemiplegic migraine | (Orphanet:569) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 | (OMIM:157300) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10 | (OMIM:610208) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11 | (OMIM:610209) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3 | (OMIM:607498) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5 | (OMIM:607508) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6 | (OMIM:607516) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | (OMIM:602481) |
MIGRAINE, FAMILIAL HEMIPLEGIC, 3 | (OMIM:609634) |
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 | (OMIM:300125) |
Sneddon syndrome | (Orphanet:820) |