Ammonia Pathways

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Displaying pathways 73 – 96 of 277 in total

Methionine Adenosyltransferase Deficiency
Methionine Adenosyltransferase Deficiency
GABA-Transaminase Deficiency
GABA-Transaminase Deficiency
Histidinemia
Histidinemia
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 3 (TYRO3)
Tyrosinemia Type 3 (TYRO3)
Sialuria or French Type Sialuria
Sialuria or French Type Sialuria
Salla Disease/Infantile Sialic Acid Storage Disease
Salla Disease/Infantile Sialic Acid Storage Disease
Tyrosine Metabolism
Tyrosine Metabolism
Glycine and Serine Metabolism
Glycine and Serine Metabolism
Porphyrin Metabolism
Porphyrin Metabolism
Pyrimidine Metabolism
Pyrimidine Metabolism
Urea Cycle
Urea Cycle
Threonine and 2-Oxobutanoate Degradation
Threonine and 2-Oxobutanoate Degradation
Acute Intermittent Porphyria
Acute Intermittent Porphyria
Porphyria Variegata (PV)
Porphyria Variegata (PV)
Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
Congenital Erythropoietic Porphyria (CEP) or Gunther Disease
Alkaptonuria
Alkaptonuria
Hawkinsinuria
Hawkinsinuria
Tyrosinemia Type I
Tyrosinemia Type I
Argininemia
Argininemia
Argininosuccinic Aciduria
Argininosuccinic Aciduria
Citrullinemia Type I
Citrullinemia Type I
Ornithine Transcarbamylase Deficiency (OTC Deficiency)
Ornithine Transcarbamylase Deficiency (OTC Deficiency)
beta-Ureidopropionase Deficiency
beta-Ureidopropionase Deficiency

Displaying pathways 73 – 96 of 277 in total