{
    "disease_id": "DOID:0111507", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "Lenz-Majewski hyperostotic dwarfism; LMHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "Lenz-Majewski syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "hyperostotic dwarfism Lenz-Majewski type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "multiple congenital anomalies, mental retardation and progressive skeletal sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "Lenz-Majewski hyperostotic dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "LMHD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007892", 
            "name": "Lenz Majewski hyperostotic dwarfism"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111507", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111507", 
            "name": "Lenz-Majewski syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111507", 
        "description": "A syndrome characterized by intellectual disability, sclerosing bone dysplasia, distinct craniofacial, dental, cutaneous and distal-limb anomalies that has_material_basis_in heterozygous mutation in PTDSS1 on chromosome 8q22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111507", 
        "name": "Lenz-Majewski hyperostotic dwarfism"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111507#disease-associations", 
            "id": "0111507", 
            "database": "Alliance of Genome Resources"
        }
    ]
}