{
    "disease_id": "DOID:14250", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "Down's syndrome - trisomy 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "Downs syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "transient myeloproliferative disorder of Down syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "G trisomy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "trisomy 21 (Down syndrome)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "Down syndrome chromosome region"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "trisomy 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "Down's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "Down syndrome critical region"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "complete trisomy 21 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "trisomy 21 syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008608", 
            "name": "leukemia, megakaryoblastic, of Down syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "Complete trisomy 21 syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "Down's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "Down's syndrome - trisomy 21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "Downs syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "G Trisomy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14250", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14250", 
            "name": "trisomy 21 syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14250", 
        "description": "A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14250", 
        "name": "Down syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14250#disease-associations", 
            "id": "14250", 
            "database": "Alliance of Genome Resources"
        }
    ]
}