{
    "disease_id": "DOID:0110943", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis, autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "autosomal recessive osteopetrosis caused by mutation in TNFSF11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "autosomal recessive malignant osteopetrosis caused by mutation in TNFSF11"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "OPTB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis, autosomal recessive 2; OPTB2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "TNFSF11 autosomal recessive osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteoclast-poor osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "TNFSF11 autosomal recessive malignant osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis autosomal recessive 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "mild autosomal recessive form osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis, autosomal recessive type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis osteoclast-poor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis, mild autosomal recessive form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "autosomal recessive osteopetrosis type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009816", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009816", 
            "name": "osteopetrosis, osteoclast-poor"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110943", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110943", 
            "name": "OPTB2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110943", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110943", 
            "name": "mild autosomal recessive form osteopetrosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110943", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110943", 
            "name": "osteoclast-poor osteopetrosis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110943", 
        "description": "An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the TNFSF11 gene on chromosome 13q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110943", 
        "name": "autosomal recessive osteopetrosis 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110943#disease-associations", 
            "id": "0110943", 
            "database": "Alliance of Genome Resources"
        }
    ]
}