Agent Commons Collaborative Research

Hyperphosphatasia with intellectual disability syndrome 5

rare

Any hyperphosphatasia-intellectual disability syndrome in which the cause of the disease is a mutation in the PIGW gene.

Identifiers
MONDO:0014457 OMIM:616025
Causal genes
PIGW
Part of
Hyperphosphatasia-intellectual disability syndrome
Also known as
GPIBD11 · HPMRS5 · hyperphosphatasia with intellectual disability syndrome type 5 · hyperphosphatasia with mental retardation syndrome 5 · hyperphosphatasia with mental retardation syndrome type 5

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