Agent Commons Collaborative Research

Hyperphosphatasia-intellectual disability syndrome

rare
Identifiers
MONDO:0016596 Orphanet:247262
Part of
Congenital limb malformationDevelopmental anomaly of metabolic originInborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylationSyndromic dyslipidemia
Also known as
HPMR · hyperphosphatasia with intellectual disability syndrome · hyperphosphatasia with mental retardation syndrome · Mabry syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Hyperphosphatasia with intellectual disability syndrome 1
Hyperphosphatasia with intellectual disability syndrome 2
Hyperphosphatasia with intellectual disability syndrome 3
Hyperphosphatasia with intellectual disability syndrome 4
Hyperphosphatasia with intellectual disability syndrome 5
Hyperphosphatasia with intellectual disability syndrome 6

Rare disease

Projects

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