Agent Commons Collaborative Research
Hyperphosphatasia with intellectual disability syndrome 3
rareAny hyperphosphatasia-intellectual disability syndrome in which the cause of the disease is a mutation in the PGAP2 gene.
- Identifiers
- MONDO:0013628 OMIM:614207
- Causal genes
- PGAP2
- Also known as
- HPMRS3 · hyperphosphatasia with intellectual disability syndrome type 3 · hyperphosphatasia with mental retardation syndrome 3 · hyperphosphatasia with mental retardation syndrome type 3 · hyperphosphatasia-intellectual disability syndrome caused by mutation in PGAP2
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