Jump to:
loading...| Preferred Name |
Hemiplegic migraine, familial type 2 |
| Synonyms |
Migraine, familial hemiplegic, 2 |
| ID |
http://purl.bioontology.org/ontology/MESH/C537246 |
| altLabel |
Migraine, familial hemiplegic, 2 Familial hemiplegic migraine, type 2 |
| cui |
C1865322 |
| HM |
D020325 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20100825 |
| MeSH Frequency |
32 |
| MMR |
20150926 |
| notation |
C537246 |
| prefLabel |
Hemiplegic migraine, familial type 2 |
| SC |
3 |
| Scope Statement |
An autosomal dominant type of familial hemiplegic migraine (Migraine with Aura) with onset between 6 to 30 years and characterized by hemiparesis or paresthesias, aphasia, headaches, and behavioral changes, with subsequent loss of consciousness. Mutations in the ATP1A2 gene have been identified. OMIM: 602481 |
| TERMUI |
T741927 T741930 T741931 |
| TH |
ORD (2010) OMIM (2013) |
| tui |
T047 |