{
    "disease_id": "DOID:0110941",
    "recommended_name": {
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        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110941",
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        "description": "An osteopetrosis characterized by autosomal recessive inheritance that has_material_basis_in homozygous or compound heterozygous mutation in the CA2 gene on chromosome 8q21."
    },
    "synonyms": [
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            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110941",
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            "url": "https://disease-ontology.org/term/DOID:0110941",
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            "url": "https://disease-ontology.org/term/DOID:0110941",
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            "name": "autosomal recessive osteopetrosis 3",
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        },
        {
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            "description": ""
        },
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            "description": ""
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            "name": "mixed renal tubular acidosis",
            "description": ""
        },
        {
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            "description": ""
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                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110941"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0110941"
}