BabelNet

bn:00205596n

Noun Concept

Categories: X-linked recessive disorders, Articles with short description, Genetic disorders, Amino acid metabolism disorders, Urea cycle

ornithine transcarbamylase deficiency ornithine carbamoyltransferase deficiency deficiency of citrulline phosphorylase OCT deficiency Ornithine Carbamoyltransferase Deficiency Disease

Ornithine transcarbamylase deficiency also known as OTC deficiency is the most common urea cycle disorder in humans. Wikipedia

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Ornithine transcarbamylase deficiency also known as OTC deficiency is the most common urea cycle disorder in humans. Wikipedia

Urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase Wikidata

A rare genetic metabolic disorder of the urea cycle. Abbreviated as OTC. Wiktionary

IS A

rare disease

metabolic syndrome

urea cycle disorder

GENETIC ASSOCIATION

ornithine transcarbamylase

HEALTH SPECIALTY

pediatrics

medical genetics

metabolic syndrome

Wikipedia

ornithine transcarbamylase deficiency

Wikidata

ornithine carbamoyltransferase deficiency

Wiktionary

ornithine transcarbamylase deficiency

Wikipedia Redirections

Ornithine carbamoyltransferase deficiency, Ornithine Carbamoyltransferase Deficiency Disease, Ornithine carbamoyltransferase deficiency disease, Ornithine transcarbamoylase deficiency, Ornithine Transcarbamylase Deficiency, Ornithine transcarbamylase deficiency, hyperammonemia due to, OTC deficiency

Wikidata Alias

deficiency of citrulline phosphorylase, OCT deficiency, Ornithine Carbamoyltransferase Deficiency, Ornithine Carbamoyltransferase Deficiency Disease, ornithine transcarbamylase deficiency, ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO, Otc Deficiency, Valproate Sensitivity