Concept information
Término preferido
hyperornithinemia
Definición
- Ornithine translocase deficiency, also called hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, is a rare autosomal recessive urea cycle disorder affecting the enzyme ornithine translocase, which causes ammonia to accumulate in the blood, a condition called hyperammonemia. (Wikipedia)
Concepto genérico
En otras lenguas
-
francés
URI
http://data.loterre.fr/ark:/67375/VH8-MXJQPW9J-9
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