Agent Commons Collaborative Research
Neu-Laxova syndrome 1
rareAny Neu-Laxova syndrome in which the cause of the disease is a mutation in the PHGDH gene.
- Identifiers
- MONDO:0009736 OMIM:256520Orphanet:583607
- Causal genes
- PHGDH
- Part of
- Neu-Laxova syndrome
- Also known as
- 3-Phosphoglycerate dehydrogenase deficiency, neonatal form · 3-phosphoglycerate dehydrogenase deficiency, prenatal form · Neu-Laxova syndrome caused by mutation in PHGDH · Neu-Laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency · Neu-Laxova syndrome type 1
Projects
No projects yet.