histidinemia
methylmalonic acidemia
ketoacidemia
inborn error of metabolism
metabolic disorder
metachromatic leukodystrophy
syndrome X
sialidosis
Chédiak-Higashi syndrome
Niemann-Pick disease
enzymopathy
metabolopathy
tyrosinemia
carnosinemia
lysine intolerance
McArdle's disease
Camurati-Engelmann disease
hyperpipecolatemia
lipochondrodystrophy
Hurler's disease
enzymopathic
Hurler's syndrome
gargoylism
dysostosis multiplex
dysmetabolism
phenylketonuria
Hartnup disease
Carpenter syndrome
plurimetabolic
homocystinuria
hypophosphatasia
adermatoglyphia
abetalipoproteinemia
trimethylaminuria
favism
autosomal recessive defect
Morquio syndrome
saccharidosis
autotoxemic
autosomal recessive disease
genetic disorder
metainflammation
mucopolysaccharidosis
metaflammation
Gilbert's syndrome
histolytic
PKU
aminoacidopathy
aspartylglucosaminuria
pseudopseudohypoparathyroidism
mannosidosis
Gaucher's disease
Zellweger syndrome
galactosemia
porphyria
McKusick-Kaufman syndrome
insulinopathy
dysfunctionality
Timothy syndrome
metabasis
hawkinsinuria
glucopenia
alkaptonuria
alcaptonuria
metabolically challenged
enzymolyze
Prader-Willi syndrome
milk intolerance
juvenile diabetes
insulinopenia
pandysautonomia
lactose intolerance
lactase deficiency
Alagille syndrome
Sandhoff disease
hypoinsulinism
autophagocytosed
lysinemia
Hurler syndrome
Lambert-Eaton myasthenic syndrome
Wiedemann-Rautenstrauch syndrome
onychopathic
decompensation
metabokine
Hunter syndrome
metaboloepigenetic
metabolotyping
Feingold syndrome
eosinophilopenia
Hermansky-Pudlak syndrome
cretin
fucosidosis
hypotrehalosemic
autosomal dominant disease
Griscelli syndrome
autosomal dominant disorder