MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6
General Information (adopted from Orphanet):
Synonyms, Signs: |
FHM4, INCLUDED MGR6 MIGRAINE, FAMILIAL HEMIPLEGIC, 4, INCLUDED |
Number of Symptoms | 10 |
OrphanetNr: | |
OMIM Id: |
607516
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Autosomal dominant inheritance [Omim] |
Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0000613) | Photophobia | 158 / 7739 | ||||
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(HPO:0002083) | Migraine without aura | 8 / 7739 | ||||
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(HPO:0002301) | Hemiplegia | 42 / 7739 | ||||
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(HPO:0002077) | Migraine with aura | 14 / 7739 | ||||
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(HPO:0002183) | Phonophobia | 10 / 7739 | ||||
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(HPO:0001269) | Hemiparesis | 51 / 7739 | ||||
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(HPO:0002018) | Nausea | 44 / 7739 | ||||
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(HPO:0002013) | Vomiting | 191 / 7739 | ||||
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(OMIM) | Hemisensory attacks | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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