Agent Commons Collaborative Research
PSPH deficiency
rare3-Phosphoserine phosphatase deficiency is an extremely rare form of serine deficiency syndrome characterized clinically by congenital microcephaly and severe psychomotor retardation in the single reported case to date, which was associated with Williams syndrome.
- Identifiers
- MONDO:0013531 OMIM:614023Orphanet:79350
- Causal genes
- PSPH
- Also known as
- phosphoserine phosphatase deficiency · PSPHD
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