Gene: [16p133/MEFV] marenostrin; Mediterranean fever (recurrent polyserositis; periodic disease); [MEF FMF ]
|
ASS |
A suggestion (Shohat-1989) that the homozygosity for one of lipocortin I (or perhaps other lipocortin) alleles accounts for familial polyserositis (Mediterranean fever) was disproved (Pras-1992)." |
|
REF |
ASS,LIN,FOG "Aksentijevich I &: AJHG, 53, 644-651, 1993a LIN,MAP "Aksentijevich I &: AJHG, 53, N2, 451-461, 1993b LIN "Aksentijevich I &: AJHG, 51, A181-181, 1992 LIN "Kastner &: CCG, 58, (HGM11), 2115, 1991 LOC,LIN,FOG "Pras &: New Engl J Med, 326, 1509-1513, 1992 PAT,FOG "Shohat &: Am J Med Genet, 34, 163-167, 1989 CLO,MAF "The French FMF Consortium: Nature Genet, 17, N1, 25-31, 1997 |
|
KEY |
imm, mfd, derm |
|
CLA |
unknown, basic |
|
LOC |
16 p13.3 |
|
MIM |
MIM: 249100 |
|
SYN |
MEF FMF |
Ссылки:
- Gene: [09q3/ITIL] inter-alpha-trypsin inhibitor, light chain (protein HC); alpha-1-microglobulin / bikunin precursor; Mediterranean fever? (HC-protein deficiency?); periodic disease? (polyserositis, recurrent; paroxysmal); [AMBP HCP ]
- Gene: [16p121/CLN3] ceroid-lipofuscinosis, neuronal 3 (juvenile amaurotic family idiocy); Batten disease (neuronal ceroid-lipofuscinosis); juvenile amaurotic family idiocy (Vogt-Spielmeyer/Sjogren disease); [BTS NCL ]
- Gene: [09q/ANX1] annexin I (lipocortin I; calpactin II; phospholipase A2 inhibitor); [p35 LPC1 ]
- Gene: [16p133/OR1F1] olfactory receptor, family 1, subfamily F, member 1; [OLFMF ]
