Disease #02866 (FHM3 (migraine, hemiplegic, familial, type 3), OMIM:609634)
Official abbreviation |
FHM3 |
Name |
migraine, hemiplegic, familial, type 3 |
OMIM ID |
609634 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SCN1A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2023-01-10 15:52:05 +01:00 (CET) |
Individuals
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