Neu-Laxova syndrome 1

MONDO:0009736

Any Neu-Laxova syndrome in which the cause of the disease is a mutation in the PHGDH gene.

Also known as: 3-Phosphoglycerate dehydrogenase deficiency, neonatal form, 3-phosphoglycerate dehydrogenase deficiency, prenatal form, Neu-Laxova syndrome 1, Neu-Laxova syndrome caused by mutation in PHGDH, Neu-Laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency, Neu-Laxova syndrome type 1, PHGDH Neu-Laxova syndrome, NLS1

28 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by