{
    "disease_id": "DOID:0060412", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "holoprosencephaly 10"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "1q41q42 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "Del(1)(q41q42)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "monosomy 1q41-q42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "1q41-q42 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "deletion 1q41-q42"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "1q41-q42 microdeletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012927", 
            "name": "monosomy 1q41q42"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060412", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060412", 
            "name": "1q41-q42 microdeletion syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060412", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060412", 
            "name": "1q41q42 microdeletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060412", 
        "description": "A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 1q41-q42 region.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060412", 
        "name": "chromosome 1q41-q42 deletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060412#disease-associations", 
            "id": "0060412", 
            "database": "Alliance of Genome Resources"
        }
    ]
}