{
    "disease_id": "DOID:0070432",
    "recommended_name": {
        "id": "DOID:0070432",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070432",
        "name": "hyperphosphatasia with impaired intellectual development syndrome 5",
        "description": "A hyperphosphatasia with impaired intellectual development syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIGW gene on chromosome 17q12."
    },
    "synonyms": [
        {
            "id": "DOID:0070432",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070432",
            "name": "GPIBD11",
            "description": ""
        },
        {
            "id": "DOID:0070432",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070432",
            "name": "HPMRS5",
            "description": ""
        },
        {
            "id": "DOID:0070432",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070432",
            "name": "hyperphosphatasia with mental retardation syndrome 5",
            "description": ""
        },
        {
            "id": "DOID:0070432",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070432",
            "name": "glycosylphosphatidylinositol biosynthesis defect 11",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia with intellectual disability syndrome 5",
            "description": "Any hyperphosphatasia-intellectual disability syndrome in which the cause of the disease is a mutation in the PIGW gene."
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "PIGW hyperphosphatasia-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia with intellectual disability syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia with intellectual disability syndrome type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia with mental retardation syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia with mental retardation syndrome type 5",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGW",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "GPIBD11",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "HPMRS5",
            "description": ""
        },
        {
            "id": "MONDO:0014457",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014457",
            "name": "glycosylphosphatidylinositol biosynthesis defect 11",
            "description": ""
        },
        {
            "id": "MIM:616025",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616025",
            "name": "Glycosylphosphatidylinositol biosynthesis defect 11",
            "description": "Glycosylphosphatidylinositol biosynthesis defect 11"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070432"
    ],
    "unlinked_id_list": []
}