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;
Origin ID : 157300;
UMLS CUI : C3887485;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
DO Cross reference
False automatic mappings
Genes related to phenotype
HPO term(s)
Semantic type(s)