{
    "disease_id": "DOID:0070080", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010943", 
            "name": "schizophrenia type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010943", 
            "name": "schizophrenia susceptibility locus, chromosome 22Q11-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010943", 
            "name": "schizophrenia 4; SCZD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010943", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010943", 
            "name": "SCZD4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070080", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070080", 
            "name": "SCZD4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070080", 
        "description": "A schizophrenia that has_material_basis_in an autosomal dominant mutation of PRODH on chromosome 22q11.21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070080", 
        "name": "schizophrenia 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070080#disease-associations", 
            "id": "0070080", 
            "database": "Alliance of Genome Resources"
        }
    ]
}