Pathways Knowlegdes

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Pathway DOIs Note
Congenital Erythropoietic Porphyria (CEP) or Gunther Disease

Accession ID: PathBank:SMP0120689
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Sarcosinemia

Accession ID: PathBank:SMP0120741
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Acute Intermittent Porphyria

Accession ID: PathBank:SMP0120447
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Dimethylglycine Dehydrogenase Deficiency

Accession ID: PathBank:SMP0120475
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Glycine and Serine Metabolism

Accession ID: PathBank:SMP0000004
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Congenital Erythropoietic Porphyria (CEP) or Gunther Disease

Accession ID: PathBank:SMP0000345
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3-Phosphoglycerate Dehydrogenase Deficiency

Accession ID: PathBank:SMP0000721
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Glycine and Serine Metabolism

Accession ID: PathBank:SMP0087245
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Porphyrin Metabolism

Accession ID: PathBank:SMP0087397
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Porphyrin Metabolism

Accession ID: PathBank:SMP0063655
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Acute Intermittent Porphyria

Accession ID: PathBank:SMP0120668
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Hereditary Coproporphyria (HCP)

Accession ID: PathBank:SMP0120712
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Porphyria Variegata (PV)

Accession ID: PathBank:SMP0120764
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3-Phosphoglycerate Dehydrogenase Deficiency

Accession ID: PathBank:SMP0120872
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Congenital Erythropoietic Porphyria (CEP) or Gunther Disease

Accession ID: PathBank:SMP0120469
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Sarcosinemia

Accession ID: PathBank:SMP0120521
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Porphyrin Metabolism

Accession ID: PathBank:SMP0121321
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Acute Intermittent Porphyria

Accession ID: PathBank:SMP0000344
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Dihydropyrimidine Dehydrogenase Deficiency (DHPD)

Accession ID: PathBank:SMP0000179
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Hyperglycinemia, Non-Ketotic

Accession ID: PathBank:SMP0000485
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