Search Ontology:
Human Disease
hyperphosphatasia with impaired intellectual development syndrome 4
- Term ID
- DOID:0070436
- Synonyms
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- glycosylphosphatidylinositol biosynthesis defect 62
- GPIBD62
- HPMRS6
- hyperphosphatasia with mental retardation syndrome 6
- Definition
- A hyperphosphatasia with impaired intellectual development syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PGAP3 gene on chromosome 17q12. https://pubmed.ncbi.nlm.nih.gov/24439110/
- References
- Ontology
- Human Disease ( DOID:0070436 )
- is a type of
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Genes Involved
Zebrafish Models