MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2
General Information (adopted from Orphanet):
| Synonyms, Signs: |
MGR2 MFTS |
| Number of Symptoms | 7 |
| OrphanetNr: | |
| OMIM Id: |
300125
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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: |
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| 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:0002077) | Migraine with aura | 14 / 7739 | ||||
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(HPO:0002183) | Phonophobia | 10 / 7739 | ||||
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(HPO:0002018) | Nausea | 44 / 7739 | ||||
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(HPO:0002013) | Vomiting | 191 / 7739 | ||||
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(HPO:0001417) | X-linked inheritance | 173 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
| Clinical Description OMIM |
Nyholt et al. (1998) studied 3 large multigenerational families in Australia in which 43 members were diagnosed with migraine, either with or without aura. Affected individuals within the pedigrees showed variation in age of onset, frequency and severity ... |