rs61752717, MEFV

N. diseases: 72
Disease: incomplete anencephaly, hemicrania ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
incomplete anencephaly, hemicrania
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
0.010 GeneticVariation BEFREE A 52-year-old Turkish man with familial Mediterranean fever (FMF) due to the homozygous M694V mutation in the MEFV-gene on chromosome 16p13.3, newly developed hemicrania, blurred and double vision, ptosis, ophthalmoparesis and peripheral facial nerve palsy. 12189462 2002