a genetic mutationcausesa problem in the complement system
a rare diseasecausesexcessive activation of the complement system
Atypical Haemolytic Uraemic Syndrome , or ... a rare diseasecausesexcessive activation of the complement system
by blood loss , low dietary levels of iron , or a disease condition that inhibits iron uptake(passive) usually caused by deficiency of iron in the system
by mutations in the C2 gene(passive) is caused byComplement component 2 deficiency
At least five mutations in the C2 gene have been foundto causecomplement component 2 deficiency
an inherited gene mutationcausesan abnormality of the immune complement system
process issuescontributeto system deficiency
Some human errorcontributedto a system deficiency
the molecular mechanismcausingthe dysregulation of the complement system
mutationscausecomplement deficiency disorders
by any one of several different alterations in the structure of complement component 2(passive) caused bya type of complement deficiency
by any one of several different alterations in the structure of complement(passive) caused bya type of complement deficiency
inside 90 % of the population(passive) is discoveredSupplement N deficiency
regionalism ... which is goingto contributecomplement the system
HAE is a genetic disorder involving lack of functional C1 esteraseleadingto overactivity of the complement system
the presence of this variant in the homozygous state in P3 and P4 ... enoughto causeLIG1 deficiency
fibromyalgia symptomsmay resultfrom a deficiency in the endocannabinoid system
Fibromyalgia could be one of thesesyndromes resultingfrom a deficiency in the Endocannabinoid system
MutationscausingVLDLR deficiency
by mutations in the FH gene(passive) is caused byFumarase deficiency
in which either codon 54 or 57 of the mannose - binding protein gene is alteredcausingdeficient complement activation
by any one of several different alterations in the structure of complement component 2(passive) caused bycomplement deficiency
Autoantibodies ... have also been describedmay causefurther complement deficiency
by any one of several different alterations in the structure of complement(passive) caused bycomplement deficiency
Polymorphism in ficolin-3 gene ( FCN3can leadto complement deficiency
by any one of several different alterations in the structure of complement component 2 ... Complement - Biology and Medicine(passive) caused bycomplement deficiency
by very poor family genes and nutrition(passive) caused bysupplement deficiencies
changes ( mutations ) in the ACADVL gene(passive) is caused byVLCAD deficiency
bad nourishment and genes(passive) caused bysupplement deficiencies
a gene change , or mutation(passive) is caused byVLCAD Deficiency
to suffering as well as other uncomfortable indicatorscan leadto suffering as well as other uncomfortable indicators
< p > Atypical hemolytic uremic syndrome ( aHUS(passive) is caused by< p > Atypical hemolytic uremic syndrome ( aHUS
diseases(passive) caused bydiseases
to accelerated amyloidleadsto accelerated amyloid
Fibromyalgia(passive) may be caused byFibromyalgia
to believe(passive) are causedto believe
to feel(passive) are caused byto feel
development of other immune functionsmay influencedevelopment of other immune functions
to accelerated amyloid plaque deposition and neurodegeneration and modulation of the microglia / macrophage phenotype in amyloid precursor protein transgenic miceleadsto accelerated amyloid plaque deposition and neurodegeneration and modulation of the microglia / macrophage phenotype in amyloid precursor protein transgenic mice
in the formation of various chemotactic agentsresultsin the formation of various chemotactic agents
to a decrease in the formation of antibody - antigen - complement immune complexesleadsto a decrease in the formation of antibody - antigen - complement immune complexes
to susceptibility to infectionleadsto susceptibility to infection
to susceptibilityleadsto susceptibility
Deficiency of regulatory proteins results in excessive complement activation that causes Complement activation pathways(passive) is composedDeficiency of regulatory proteins results in excessive complement activation that causes Complement activation pathways