Migraine with or without aura, susceptibility to, 6

Preferred Label : Migraine with or without aura, susceptibility to, 6;

CISMeF acronym : FHM4; MGR6;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MGR6;

Included titles and symbols : Migraine, familial hemiplegic, 4; FHM4;

Description : For a phenotypic description and discussion of genetic heterogeneity of migraine headaches, see MGR1 (157300).;

Inheritance : Autosomal dominant;

Prefixed ID : %607516;

Details

Origin ID

607516;

UMLS CUI

C1843765;

Automatic exact mappings (from CISMeF team)
- Familial or sporadic hemiplegic migraine [ORDO Disease]
- migraine, familial hemiplegic, 4 [MeSH concept]
- migraine, familial hemiplegic, 4 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Hemiparesis [HPO term]
- Hemiplegia [HPO term]
- Migraine with aura [HPO term]
- Migraine without aura [HPO term]
- Nausea [HPO term]
- Phonophobia [HPO term]
- Photophobia [HPO term]
- Vomiting [HPO term]
ORDO concept(s)
- Familial or sporadic hemiplegic migraine [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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