{
    "disease_id": "DOID:0110940", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "SNX10 autosomal recessive osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "OPTB8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "SNX10 autosomal recessive malignant osteopetrosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "osteopetrosis, autosomal recessive 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "autosomal recessive osteopetrosis caused by mutation in SNX10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "autosomal recessive malignant osteopetrosis caused by mutation in SNX10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "osteopetrosis, autosomal recessive 8; OPTB8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "osteopetrosis, autosomal recessive type 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014040", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014040", 
            "name": "autosomal recessive osteopetrosis type 8"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110940", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110940", 
            "name": "OPTB8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110940", 
        "description": "An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous mutation in the SNX10 gene on chromosome 7p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110940", 
        "name": "autosomal recessive osteopetrosis 8"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110940#disease-associations", 
            "id": "0110940", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
