Zellweger syndrome
abetalipoproteinemia
hepatopericardial
syndrome X
renopericardial
hepatosteatosis
apoform
metabolic disorder
proapolipoprotein
homocystinuria
nonperimesencephalic
Hurler's disease
apomeiotic
inborn error of metabolism
Hurler's syndrome
dysostosis multiplex
gargoylism
lipochondrodystrophy
peroxin
plurimetabolic
sitosterolemia
pericarditis
chemical peritonitis
aperistalsis
hypobetalipoproteinemia
analphalipoproteinemia
pexophagy
aminoacidopathy
hyperpipecolatemia
methylmalonic acidemia
peracid
perinatological
nephropyosis
Niemann-Pick disease
macropexophagy
hypoperistalsis
apocryphally
heart sac
theca cordis
-exia
hyperlipoproteinemia
alkaptonuria
familial hypercholesterolemia
alcaptonuria
Alagille syndrome
peracidic
perthiocyanogen
choleperitonitis
sulphocyanogen
periphytivore
hydroxanthic
cardiac tamponade
dyshepatia
metabasis
perissodactylism
peristaltism
periplasmically
apotarget
peritheliomatous
pericardioperitoneal
peroxyacid
prepericardial
metabolopathy
phenylketonuria
histidinemia
extrapericardial
prepericardiac
hepatopathy
Morison's pouch
apoplasmic
periplastidic
ectodermosis
lipidosis
hyperpericardium
carnosinemia
hyperlipaemia
ketoacidemia
apotheotic
granulomatosis infantiseptica
apophatically
perbromic
periapses
hypocholesterolemia
peroxyacetic acid
dermo
hypercholanemic
pericholecystitic
hyperlipoidemia
perineuritis
lactoperoxidase
periphysate
galactosemia
pyopericarditis
perichoretic
micropexophagy
abominatio
erythrohepatic
neurosome

English words for 'A rare congenital disorder characterized by the reduction or absence of peroxisomes in the cells of the liver, kidneys, and brain and the inability to beta-oxidize very-long-chain fatty acids.'

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