familial hemiplegic migraine
Information
- Disease name
- familial hemiplegic migraine
- Disease ID
- DOID:0060178
- Description
- "A migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body (hemiparesis). Additional features of an aura can include difficulty with speech, confusion, and drowsiness." [url:http\://ghr.nlm.nih.gov/condition/familial-hemiplegic-migraine]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00358839 | Completed | N/A | Calcitonin Gene Related Peptide-Induced Headache in Patients With Familial Hemiplegic Migraine Type 1 and 2. | July 2006 | October 2006 |
| NCT00541736 | Completed | N/A | Glyceryl-Trinitrate-Induced Headache in Patients With Familial Hemiplegic Migraine | October 2007 | May 2008 |
| NCT00687947 | Completed | N/A | Calcitonin Gene-related Peptide in Familial Hemiplegic Migraine (FHM) and Migraine With Aura (MA) | May 2008 | August 2008 |
- Disase is a (Disease Ontology)
- DOID:10024
- Cross Reference ID (Disease Ontology)
- GARD:10975
- Cross Reference ID (Disease Ontology)
- ICD10CM:G43.8
- Cross Reference ID (Disease Ontology)
- ICD9CM:346.8
- Cross Reference ID (Disease Ontology)
- ORDO:569
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:193037008
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0477373
- MedGen concept unique identifier (MedGen Concept name)
- C0338484
- MedGen unique identifier (MedGen Concept name)
- 87374