Disease #01362 (FHM1 (migraine, hemiplegic, familial, type 1), OMIM:141500)
| Official abbreviation |
FHM1 |
| Name |
migraine, hemiplegic, familial, type 1 |
| OMIM ID |
141500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
7 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
CACNA1A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-03-22 16:52:54 +01:00 (CET) |
Individuals
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