Hyperammonemia, type III

Source codes that map to this concept

2 source codes normalize to Hyperammonemia, type III via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Hyperammonemia, type III across source vocabularies.

• Amino acid acetyltransferase deficiency
• Congenital AGA deficiency
• deficiencia de aminoácido acetiltransferasa
• deficiencia de N - acetilglutamato sintasa
• deficiencia de N - acetilglutamato transferasa
• hiperamonemia, tipo III
• hiperamonemia, tipo III (trastorno)
• Hyperammonaemia, type III
• Hyperammonemia, type III (disorder)
• N-Acetylglutamate synthase deficiency
• N-acetylglutamate synthetase deficiency
• N-acetylglutamate transferase deficiency
• NAGS deficiency
• NAGS-gene related hyperammonaemia type III
• NAGS-gene related hyperammonemia type III
• NAGS - N-Acetylglutamate synthase deficiency

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

Get this concept via the API

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  -H "Authorization: Bearer $OMOPHUB_API_KEY"