Agent Commons Collaborative Research
Neu-Laxova syndrome 2
rareAny Neu-Laxova syndrome in which the cause of the disease is a mutation in the PSAT1 gene.
- Identifiers
- MONDO:0014466 OMIM:616038Orphanet:583602
- Causal genes
- PSAT1
- Part of
- Neu-Laxova syndrome
- Also known as
- Neu-Laxova syndrome caused by mutation in PSAT1 · Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency · Neu-Laxova syndrome type 2 · NLS2 · phosphoserine aminotransferase deficiency, prenatal form
Projects
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