MCID: MGR042
MIFTS: 11

Migraine with or Without Aura 13

Categories: Genetic diseases

Aliases & Classifications for Migraine with or Without Aura 13

MalaCards integrated aliases for Migraine with or Without Aura 13:

Name: Migraine with or Without Aura 13 57 75
Migraine, with or Without Aura 13 57 29 6 40
Migraine, with or Without Aura, Susceptibility to, 13 57 13
Mgr13 57 75
Migraine with or Without Aura, Susceptibility to, 13 57

Classifications:



External Ids:

OMIM 57 613656
MedGen 42 C3150908

Summaries for Migraine with or Without Aura 13

UniProtKB/Swiss-Prot : 75 Migraine with or without aura 13: A form of migraine transmitted in an autosomal dominant pattern. Migraine is a disabling symptom complex of periodic headaches, usually temporal and unilateral. Headaches are often accompanied by irritability, nausea, vomiting and photophobia, preceded by constriction of the cranial arteries. The two major subtypes are common migraine (migraine without aura) and classic migraine (migraine with aura). Classic migraine is characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred vision, hallucinations, vertigo, numbness and difficulty in concentrating and speaking.

MalaCards based summary : Migraine with or Without Aura 13, also known as migraine, with or without aura 13, is related to migraine with or without aura 1. An important gene associated with Migraine with or Without Aura 13 is KCNK18 (Potassium Two Pore Domain Channel Subfamily K Member 18).

Description from OMIM: 613656

Related Diseases for Migraine with or Without Aura 13

Diseases related to Migraine with or Without Aura 13 via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 migraine with or without aura 1 11.0

Symptoms & Phenotypes for Migraine with or Without Aura 13

Clinical features from OMIM:

613656

Drugs & Therapeutics for Migraine with or Without Aura 13

Search Clinical Trials , NIH Clinical Center for Migraine with or Without Aura 13

Genetic Tests for Migraine with or Without Aura 13

Genetic tests related to Migraine with or Without Aura 13:

# Genetic test Affiliating Genes
1 Migraine, with or Without Aura 13 29 KCNK18

Anatomical Context for Migraine with or Without Aura 13

Publications for Migraine with or Without Aura 13

Variations for Migraine with or Without Aura 13

ClinVar genetic disease variations for Migraine with or Without Aura 13:

6
# Gene Variation Type Significance SNP ID Assembly Location
1 KCNK18 NM_181840.1(KCNK18): c.414_415delCT (p.Phe139Trpfs) deletion Likely pathogenic rs869025175 GRCh37 Chromosome 10, 118969069: 118969070
2 KCNK18 NM_181840.1(KCNK18): c.414_415delCT (p.Phe139Trpfs) deletion Likely pathogenic rs869025175 GRCh38 Chromosome 10, 117209558: 117209559
3 KCNK18 NM_181840.1(KCNK18): c.361dupT (p.Tyr121Leufs) duplication Likely pathogenic rs541915908 GRCh37 Chromosome 10, 118969016: 118969016
4 KCNK18 NM_181840.1(KCNK18): c.361dupT (p.Tyr121Leufs) duplication Likely pathogenic rs541915908 GRCh38 Chromosome 10, 117209505: 117209505

Expression for Migraine with or Without Aura 13

Search GEO for disease gene expression data for Migraine with or Without Aura 13.

Pathways for Migraine with or Without Aura 13

GO Terms for Migraine with or Without Aura 13

Sources for Migraine with or Without Aura 13

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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