{
    "disease_id": "DOID:0110938",
    "recommended_name": {
        "id": "DOID:0110938",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110938",
        "name": "autosomal dominant osteopetrosis 2",
        "description": "An osteopetrosis characterized by autosomal dominant inheritance of sclerosis predominantly involving the spine, the pelvis, and the skull base, bone fragility and dental abscesses that has_material_basis_in mutation in the CLCN7 gene on chromosome 16p13."
    },
    "synonyms": [
        {
            "id": "DOID:0110938",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110938",
            "name": "Albers-Schonberg osteopetrosis",
            "description": ""
        },
        {
            "id": "DOID:0110938",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110938",
            "name": "OPTA2",
            "description": ""
        },
        {
            "id": "DOID:0110938",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110938",
            "name": "autosomal dominant Albers-Schonberg disease",
            "description": ""
        },
        {
            "id": "DOID:0110938",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110938",
            "name": "autosomal dominant osteopetrosis type II",
            "description": ""
        },
        {
            "id": "DOID:0110938",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110938",
            "name": "osteopetrosis autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "autosomal dominant osteopetrosis 2",
            "description": "A sclerosing disorder of the skeleton characterized by increased bone density that classically displays the radiographic sign of ''sandwich vertebrae'' (dense bands of sclerosis parallel to the vertebral endplates)."
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "Albers-Schnberg osteopetrosis",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "OPTA2",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "autosomal dominant osteopetrosis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "osteopetrosis autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "osteopetrosis, autosomal dominant type 2",
            "description": ""
        },
        {
            "id": "MONDO:0008156",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008156",
            "name": "osteopetrosis, autosomal dominant 2",
            "description": ""
        },
        {
            "id": "MIM:166600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/166600",
            "name": "Osteopetrosis, autosomal dominant 2",
            "description": "Osteopetrosis, autosomal dominant 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110938"
    ],
    "unlinked_id_list": []
}