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Standards Ontologies Notations
familial hemiplegic migraine 3

Summary
Synonym
  • FHM3
  • MHP3
Definition
A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3.
Super Class
familial hemiplegic migraine
Disease Ontology
DOID:0111183
Mondo Disease Ontology
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6323 SCN1A sodium voltage-gated channel alpha subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
20265 Scn1a sodium channel, voltage-gated, type I, alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
81574 Scn1a sodium voltage-gated channel alpha subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
32619 para paralytic
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024