Noun:

జీవక్రియ యొక్క పుట్టుకతో వచ్చిన లోపం,

inborn error of metabolism's Usage Examples:

of purine–pyrimidine metabolism are a class of inborn error of metabolism disorders specifically affecting purine metabolism and pyrimidine metabolism.

Glutathionuria is the presence of glutathione in the urine, and is a rare inborn error of metabolism.

Ethylmalonic encephalopathy (EE) is a rare autosomal recessive inborn error of metabolism.

Genetic GSD is caused by any inborn error of metabolism (genetically defective enzymes) involved in these processes.

Glucose-6-phosphate dehydrogenase deficiency (G6PDD) is an inborn error of metabolism that predisposes to red blood cell breakdown.

deficiency (LAL deficiency or LAL-D), is an autosomal recessive inborn error of metabolism that results in the body not producing enough active lysosomal.

2,4 Dienoyl-CoA reductase deficiency is an inborn error of metabolism resulting in defective fatty acid oxidation caused by a deficiency of the enzyme.

dehydrogenase deficiency (G6PDD) is an inborn error of metabolism that predisposes to red blood cell breakdown.

been reclassified as a benign inborn error of metabolism.

first patient with isolated pancreatic trypsinogen deficiency, an inborn error of metabolism, that became known as trypsinogen deficiency disease.

Aminoacylase 1 deficiency is a rare inborn error of metabolism.

Inborn errors of carbohydrate metabolism are inborn error of metabolism that affect the catabolism and anabolism of carbohydrates.

Lysosomal acid lipase deficiency (LAL deficiency or LAL-D), is an autosomal recessive inborn error of metabolism that results in the body not producing.

Synonyms:

foul,

Antonyms:

fair, unclassified,