{
    "disease_id": "DOID:0111063",
    "recommended_name": {
        "id": "DOID:0111063",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111063",
        "name": "hyperphosphatemic familial tumoral calcinosis",
        "description": "A calcinosis characterized by autosomal recessive inheritance of elevated blood calcium levels and calcium phosphate crystals in cutaneous and subcutaneous tissues that has_material_basis_in mutation in the GALNT3 gene, the FGF23 gene, or the KL gene."
    },
    "synonyms": [
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "HFTC",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "PHPTC",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "cortical hyperostosis with hyperphosphatemia",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "familial Teutschlaender disease",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "hypercalcemic tumoral calcinosis",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "hyperostosis with hyperphosphatemia",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "hyperphosphatemia hyperostosis",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "hyperphosphatemia hyperostosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "hyperphosphatemia tumoral calcinosis",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "lipocalcinogranulomatosis",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "morbus Teutschlaender",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "primary hyperphosphatemic tumoral calcinosis",
            "description": ""
        },
        {
            "id": "DOID:0111063",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111063",
            "name": "tumoral calcinosis with hyperphosphatemia",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, hyperphosphatemic, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "HFTC",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "HFTC1",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "Morbus Teutschlaender",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "Teutschlaender disease, familial",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "calcinosis, tumoral, with hyperphosphatemia",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "hyperostosis-hyperphosphatemia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, HYPERPHOSPHATEMIC, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, Hyperphosphatemic, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, hyperphosphatemic, familial",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, hyperphosphatemic, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0100252",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0100252",
            "name": "tumoral calcinosis, primary Hyperphosphatemic",
            "description": ""
        },
        {
            "id": "MIM:211900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/211900",
            "name": "Tumoral calcinosis, hyperphosphatemic, familial, 1",
            "description": "Tumoral calcinosis, hyperphosphatemic, familial, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111063"
    ],
    "unlinked_id_list": []
}