Migraine with or without aura, susceptibility to, 1

Preferred Label : Migraine with or without aura, susceptibility to, 1;

CISMeF acronym : MA; MGR1;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : MIGRAINE; Mgau; MA; MGR1;

Description : Migraine is the most common type of chronic, episodic headache, as summarized by Featherstone (1985). One locus for migraine with or without aura (MGR1) has been identified on chromosome 4q24. Other loci for migraine have been identified on 6p21.1-p12.2 (MGR3; 607498), 14q21.2-q22.3 (MGR4; 607501), 19p13 (MGR5; 607508), 1q31 (MGR6; 607516), 15q11-q13 (MGR7; 609179), 5q21 (with or without aura, MGR8, 609570; with aura, MGR9, 609670), 17p13 (MGR10; 610208), 18q12 (MGR11; 610209), 10q22-q23 (MGR12; 611706), and the X chromosome (MGR2; 300125). Mutation in the KCNK18 gene (613655) on chromosome 10q25 causes migraine with aura (MGR13; 613656). A subtype of autosomal dominant migraine with aura (MA), familial hemiplegic migraine (FHM; see 141500), is caused by mutation in the;

Inheritance : Autosomal dominant;

Prefixed ID : %157300;

Détails

Origin ID

157300;

UMLS CUI

C3887485;

Automatic exact mappings (from CISMeF team)
- AML Molecular Analysis Table [NCIt concept]
- EWS Molecular Analysis Table [NCIt concept]
- Ma+Ta Ab [LOINC component]
- Macroscopic Findings Domain [NCIt concept]
- Man Chinese [NCIt concept]
- Migraine aura [MedDRA LLT]
- Migraine, unspecified [ICD-9 code]
- Milliampere [NCIt concept]
- Missed abortion [ICD-11 Category]
- Other forms of migraine [ICD-9 code]
- Other migraine [ICD-10 Sub-category (who)]
- alzheimer disease [MeSH Descriptor]
- forelimb [MeSH Descriptor]
- meta-analysis as topic [MeSH Descriptor]
- microtubule organizing center attachment site [GO term]
Currated CISMeF NLP mapping
- MIGRAINE [WHO-ART High Level Term]
- Migraine [PASCAL descriptor]
- Migraine [ICD-10 category]
- Migraine [ICD-11 Category]
- Migraine [ICD-10 category (who)]
- Migraine [HPO term]
- Migraine [ICNP subject]
- Migraine [MedDRA Preferred Term]
- Migraine [NCIt concept]
- Migraine [ICD-9 code]
- Migraine (disorder) [SNOMED CT concept]
- Migraine Disorders [DeCS]
- Migraine NOS [MedDRA LLT]
- Migraine headache [MedDRA LLT]
- Migraine, unspecified [ICD-10 Sub-category]
- Sick headache (disorder) [SNOMED CT concept]
- migraine [Disease (Nov.)]
- migraine [DO Concept]
- migraine [ICPC-2 Rubric]
- migraine [MedlinePlus Topic]
- migraine disorders [MeSH Descriptor]
- migraine disorders [MeSH concept]
- migraine, nos [SNOMED Notion]
- sick headache [MeSH concept]
DO Cross reference
- migraine [DO Concept]
False automatic mappings
- Bioconductor caAffy MAS Probe Summary Method [NCIt concept]
- Doxorubicin/Mitomycin [NCIt concept]
- MAS1 wt Allele [NCIt concept]
- Madagascar [NCIt concept]
- Massachusetts [NCIt concept]
- Master of Arts [NCIt concept]
- McCune-Albright Syndrome [NCIt concept]
- Meconium Aspiration Syndrome [NCIt concept]
- Morocco [NCIt concept]
- mA (qualifier value) [Inactive SNOMED CT concept]
Genes related to phenotype
- Endothelin receptor, type a [OMIM gene]
- Estrogen receptor 1 [OMIM gene]
- Tumor necrosis factor [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Migraine with aura [HPO term]
- Migraine without aura [HPO term]
- Nausea [HPO term]
- Phonophobia [HPO term]
- Photophobia [HPO term]
- Vomiting [HPO term]
Semantic type(s)
- Finding [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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