Gamma-glutamylcysteine synthetase deficiency

MONDO:0009259

A disorder that is principally characterized by hemolytic anemia, (usually rather mild), however, the presence of neurological symptoms has also been reported.

Also known as: anemia, congenital, nonspherocytic hemolytic, 7, gamma-glutamylcysteine synthetase deficiency, hemolytic anaemia due to, gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to, glutamate-cysteine ligase deficiency, hemolytic anaemia due to gamma-glutamylcysteine synthetase deficiency, inborn error of glutamate-cysteine ligase activity, inborn glutamate-cysteine ligase activity disorder, rare inborn error of glutamate-cysteine ligase activity

23 clinical trials for this condition and its sub-types, 0 tagged with Gamma-glutamylcysteine synthetase deficiency itself.

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↑ Anemia due to enzyme disorder (14) ↑ Congenital nonspherocytic hemolytic anemia (12) ↑ Inherited glutathione metabolism disease (1)

Including sub-types (23) Tagged with Gamma-glutamylcysteine synthetase deficiency (0)

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