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| Term | serine deficiency | ID (Ontology) | DOID:0050721 (Human Disease) |
| Definition | An amino acid metabolic disorder that has_material_basis_in defects in the biosynthesis of the amino acid L-serine. | ||
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inherited metabolic disorder |__amino acid metabolic disorder |__serine deficiency 4 rec. |__Neu-Laxova syndrome 1 1 rec. |__Neu-Laxova syndrome 2 1 rec. |__PHGDH deficiency 2 rec. |__PSAT deficiency 1 rec. |__PSPH deficiency 1 rec. |
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| Is a | amino acid metabolic disorder | ||
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