{
    "disease_id": "DOID:0110913",
    "recommended_name": {
        "id": "DOID:0110913",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110913",
        "name": "adult hypophosphatasia",
        "description": "A hypophosphatasia that has_material_basis_in a heterozygous or compound heterozygous mutation of the ALPL gene on chromosome 1p36.12."
    },
    "synonyms": [
        {
            "id": "DOID:0110913",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110913",
            "name": "mild hypophosphatasia",
            "description": ""
        },
        {
            "id": "MONDO:1010154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010154",
            "name": "adult hypophosphatasia",
            "description": "Adult hypophosphatasia (A-HPP) is a mildform of hypophosphatasia characterized by osteomalacia, chondrocalcinosis, osteoarthropathy, stress fractures duringmiddle age, and dental anomalies."
        },
        {
            "id": "MONDO:1010154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010154",
            "name": "adult hypophosphatasia",
            "description": ""
        },
        {
            "id": "MONDO:1010154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:1010154",
            "name": "hypophosphatasia of adults",
            "description": ""
        },
        {
            "id": "MIM:146300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/146300",
            "name": "Hypophosphatasia",
            "description": "Hypophosphatasia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110913"
    ],
    "unlinked_id_list": []
}