{
    "disease_id": "DOID:0111781", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "early-onset parkinsonism-intellectual disability syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "WSMN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "basal ganglion disorder with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "Wsn"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "Laxova-Opitz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "BGMR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "WAISMAN syndrome; WSMN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "Parkinsonism, early onset with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "Parkinsonism, early-onset, with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "Laxova Brown hogan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "basal ganglia disorder with mental retardation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010709", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010709", 
            "name": "X-linked recessive basal ganglia disorder with mental retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111781", 
            "name": "Laxova-Opitz syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111781", 
            "name": "early-onset parkinsonism-intellectual disability syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111781", 
        "description": "A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that has_material_basis_in hemizygous or homozygous mutation in RAB39B on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111781", 
        "name": "Waisman syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111781#disease-associations", 
            "id": "0111781", 
            "database": "Alliance of Genome Resources"
        }
    ]
}