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DO Term : familial hemiplegic migraine 3 [DOID:0111183] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hemiplegic migraine that has_material_basis_in heterozygous mutation in SCN1A on 2q24.3.

synonyms:
FHM3,
609634,
OMIM:609634,
GARD:10974,
MHP3

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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