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