{
    "disease_id": "DOID:0110937", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "autosomal dominant osteopetrosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis, autosomal dominant 1; OPTA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis (disease) caused by mutation in LRP5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "OPTA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "LRP5 osteopetrosis (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011877", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011877", 
            "name": "osteopetrosis, autosomal dominant, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110937", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110937", 
            "name": "OPTA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110937", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110937", 
            "name": "autosomal dominant osteopetrosis type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110937", 
        "description": "An osteopetrosis characterized by autosomal dominant inheritance of generalized osteosclerosis that is most pronounced in the cranial vault, absence of increased fractures and has_material_basis_in heterozygous mutation in the LRP5 gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110937", 
        "name": "autosomal dominant osteopetrosis 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110937#disease-associations", 
            "id": "0110937", 
            "database": "Alliance of Genome Resources"
        }
    ]
}