Noun:

বিপাক সহজাত ত্রুটি,

inborn error of metabolism's Usage Examples:

Aminoacylase 1 deficiency is a rare inborn error of metabolism.

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

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

An inborn error of steroid metabolism is an inborn error of metabolism due to defects in steroid metabolism.

Leukotriene C4 synthase deficiency is an inborn error of metabolism.

been reclassified as a benign inborn error of metabolism.

Histidinemia occurs as the result of an inborn error of metabolism that may result in either an.

people have been reported in the medical literature with this inborn error of metabolism.

disease and a glycogen storage disorder that is caused by an inborn error of metabolism.

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

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

test can be used to exclude the possibility that a person has an inborn error of metabolism, usually one of the organic acidemias.

Cytochrome P450 oxidoreductase deficiency (PORD) is a rare disease and inborn error of metabolism caused by deficiency of cytochrome P450 oxidoreductase (POR).

is a form of glycogen storage disease, which is caused by an inborn error of metabolism.

disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism (specifically of carbohydrates) characterized by a deficiency.

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.

Sialuria is a rare inborn error of metabolism characterized by cytoplasmic accumulation and increased urinary.

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

For more online resources and references, see inborn error of metabolism.

Synonyms:

foul;

Antonyms:

fair; unclassified;