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by mutations in the HFE gene(passive) caused byHereditary Haemochromatosis
abnormal amyloid protein , transthyretin , which are produced in the liver(passive) is caused byHereditary amyloidosis
by abnormal amyloid protein , transthyretin , which are produced in the liver(passive) is caused byHereditary amyloidosis
a hereditary mutation of the TTR gene(passive) is caused byHereditary amyloidosis
pathogenic single - nucleotide variants in the gene encoding transthyretin ( TTR ) that induce transthyretin misfolding and systemic deposition of amyloid(passive) is caused byHereditary transthyretin amyloidosis
by mutation in TTR gene(passive) caused byhereditary amyloidosis
transthyretin Leu55Pro mutation(passive) caused byhereditary transthyretin amyloidosis
pathogenic single - nucleotide variants in the gene encoding transthyretin ( TTR(passive) is caused byHereditary transthyretin amyloidosis
The transthyretin protein ... this proteincauseshereditary amyloidosis
A new deletion mutation of the apolipoprotein AI genecausinghereditary amyloidosis
by an abnormal gene(passive) is caused byHereditary amyloidosis
Several abnormal or mutant genescan causehereditary amyloidosis
by mutations affecting other proteins(passive) caused byhereditary amyloidosis
several abnormal genescan causehereditary amyloidosis
the apolipoprotein AI genecausinghereditary amyloidosis
# # # Mutationcausinghereditary amyloidosis
Mutationcausinghereditary amyloidosis
The first deletion mutationscausinghereditary amyloidosis
by an abnormality mutation in gene transthyretin(passive) caused byhereditary amyloidosis
by a frame - shift mutation in fibrinogen Aalpha - chain gene(passive) caused byhereditary amyloidosis
by inherited genetic mutation(passive) is caused byHereditary Amyloidosis
a TPO gene mutation(passive) caused byhereditary thrombocytosis
Inherited Genetic Mutations By(passive) s ... Is Primarily Caused byHereditary Amyloidosis
by mutations in the spectrin gene(passive) caused byhereditary elliptocytosis
The mutationcan causehereditary anemias
genetic mutations(passive) can be caused byHereditary amyloidosis
genetic mutations(passive) can be caused by Hereditary amyloidosis
A new apolipoprotein Al variant , Trp50Argcauseshereditary amyloidosis
titin mutationscausinghereditary myopathy
by frame - shift mutation in fibrinogen(passive) caused byhereditary amyloidosis
alterations in other genes ... not yet identified(passive) can be caused byhereditary thrombocytosis
by genetic mutations in different genes(passive) can be caused byHereditary amyloidosis
genetic mutations in different genes(passive) can be caused byHereditary amyloidosis
by inheriting a gene mutation(passive) are caused byHereditary amyloidosis
by mutations in the [ [ spectrin(passive) caused byhereditary elliptocytosis
by R554L fibrinogen A alpha - chain mutation in a Spanish family and review of the literature(passive) caused byHereditary amyloidosis
frequently(passive) is ... causedHereditary FSGS
deficiencycauseshereditary coproporphyria)[40
mutationscausinghereditary elliptocytosis
R554L fibrinogen Aalpha - chain mutation in a Spanish family and review of the literature(passive) caused byHereditary amyloidosis
swelling of the face , arms , legs , throat , windpipe , bowels , or sexual organscausesswelling of the face , arms , legs , throat , windpipe , bowels , or sexual organs
swelling of the face , arms , legs , throat , windpipe , bowels , or sexual body organscausesswelling of the face , arms , legs , throat , windpipe , bowels , or sexual body organs
swelling of the face , arms , legs , throat , windpipe , bowels , orcausesswelling of the face , arms , legs , throat , windpipe , bowels , or
swelling of the face , arms , legs , throat , windpipecausesswelling of the face , arms , legs , throat , windpipe
your body to absorb too much iron from the food you eatcausesyour body to absorb too much iron from the food you eat
swelling of the face , arms , legs , neck , windpipe , bowels , or sexual organscausesswelling of the face , arms , legs , neck , windpipe , bowels , or sexual organs
swelling of the face , arms , legs , throatcausesswelling of the face , arms , legs , throat
in a heartbeat that is too fast , too slow or irregularcan resultin a heartbeat that is too fast , too slow or irregular
attacks of swelling and symptoms such as stomach problems or trouble breathingcan causeattacks of swelling and symptoms such as stomach problems or trouble breathing
swelling of the face , extremitiescausesswelling of the face , extremities
swelling of your facecausesswelling of your face
An increasing degree of deafness ,(passive) caused byAn increasing degree of deafness ,
episodes of swelling of the facecausesepisodes of swelling of the face
episodes of severe swellingcausesepisodes of severe swelling
swelling of the face , armscausesswelling of the face , arms
swelling ofcausesswelling of
episodes of swelling of thecausesepisodes of swelling of the
swelling anywhere in the bodycan causeswelling anywhere in the body
swelling most peoplecausesswelling most people
attacks of swelling and symptoms like stomach problems or breathing difficultiesmay causeattacks of swelling and symptoms like stomach problems or breathing difficulties
her body to swell Itcausesher body to swell It
painful swelling swelling anywhere in the body and sometimes difficulty breathingcausespainful swelling swelling anywhere in the body and sometimes difficulty breathing
edema or swelling when I have flarescausesedema or swelling when I have flares
before C1 inhibitor deficiencycausedbefore C1 inhibitor deficiency
swelling in parts of the body and can be fatalcausesswelling in parts of the body and can be fatal
acute edema attacks(passive) caused byacute edema attacks
an accumulation of ironcausesan accumulation of iron
Excess iron(passive) is usually caused byExcess iron
these severe , recurring and disfiguring attacks of swelling across the bodycausesthese severe , recurring and disfiguring attacks of swelling across the body
By C1-Esterase Inhibitor DeficiencyCausedBy C1-Esterase Inhibitor Deficiency
Abdominal pain(passive) caused byAbdominal pain
from inherited partial C1 inhibitor deficiencyresultingfrom inherited partial C1 inhibitor deficiency
a hand(passive) caused bya hand
per weekcausesper week
cirrhosis(passive) caused bycirrhosis
from a quantitative or qualitative deficiency of the C1 esterase inhibitor ( C1-INHresultsfrom a quantitative or qualitative deficiency of the C1 esterase inhibitor ( C1-INH
from excessive production of bradykininresultsfrom excessive production of bradykinin
by blocking the treatmentcausedby blocking the treatment
to alexithymia in childrenledto alexithymia in children
gastrointestinal swellings or intussusceptions(passive) caused bygastrointestinal swellings or intussusceptions