{
    "disease_id": "DOID:0110946",
    "recommended_name": {
        "id": "DOID:0110946",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110946",
        "name": "autosomal recessive osteopetrosis 7",
        "description": "An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the TNFRSF11A gene on chromosome 18q21."
    },
    "synonyms": [
        {
            "id": "DOID:0110946",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110946",
            "name": "osteoclast-poor osteopetrosis with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "DOID:0110946",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110946",
            "name": "OPTB7",
            "description": ""
        },
        {
            "id": "DOID:0110946",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110946",
            "name": "autosomal recessive osteopetrosis type 7",
            "description": ""
        },
        {
            "id": "DOID:0110946",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110946",
            "name": "osteopetrosis-hypogammaglobulinemia syndrome",
            "description": ""
        },
        {
            "id": "DOID:0110946",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110946",
            "name": "autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "autosomal recessive osteopetrosis 7",
            "description": "Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the TNFRS11A gene."
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "OPTB7",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "TNFRSF11A osteopetrosis (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "autosomal recessive osteopetrosis type 7",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis (disease) caused by mutation in TNFRSF11A",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis, autosomal recessive type 7",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis-hypogammaglobulinemia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis autosomal recessive 7",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis osteoclast-poor with hypogammaglobulinemia",
            "description": ""
        },
        {
            "id": "MONDO:0012859",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012859",
            "name": "osteopetrosis, autosomal recessive 7",
            "description": ""
        },
        {
            "id": "MIM:612301",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612301",
            "name": "Osteopetrosis, autosomal recessive 7",
            "description": "Osteopetrosis, autosomal recessive 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110946"
    ],
    "unlinked_id_list": []
}