huntingtin
Huntingtonism
tominersen
oligoglutamine
tafamidis
parkin
tauopathy
vutrisiran
pathoprogression
Alzheimer's syndrome
foldopathy
A-68
candidate
vCJD
calmyrin
pathophenotype
proteinosis
Huntington
George Huntington
paraamyloidosis
priliximab
norrin
Alzies
globulomer
proamyloid
pathogenetics
coindicant
McArdle's disease
patisiran
cohesinopathy
hyperbetalipoproteinemia
homocystinuria
dardarin
proteopathy
amyloidolytic
Pick body
neuroprotein
amyloidogenic
chromoshadow
neurofibromin
proamyloidogenic
synphilin
metabolopathy
chytridiosis
syndrome X
diagnostic
septin
SET
Rho
inborn error of metabolism
Hartnup disorder
microspecies
ketoacidemia
amylophagic
vorarephile
pathophenotypic
parkinsonoid
ponezumab
metaproteogenomic
amyloidotic
histidinemia
pseudosclerosis
seromarker
crenezumab
Alagille syndrome
moesin
radixin
neopathy
envoplakin
Turner
metabasis
modificomics
pleiohomeotic
proteoform
autosomal dominant disorder
phenylketonuria
metainflammation
shmoose
amyloid
necroenzyme
organic defect
autosomal dominant disease
genetic abnormality
enzymopathic
nonsyntaxin
choreiform movement
inherited disease
genetic defect
inherited disorder
Burnettian
genetic disorder
congenital disease
hereditary disease
cholix
gantenerumab
plaque
signalosome
hereditary condition
pathobiotype
genetic disease

English words for 'A protein whose polymorphism is associated with Huntington's disease.'

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