{
    "disease_id": "DOID:0060580", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "Noonan syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "NS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "autosomal recessive Noonan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "Noonan syndrome autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "Noonan syndrome, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011531", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011531", 
            "name": "Noonan syndrome 2; NS2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060580", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060580", 
            "name": "NS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060580", 
        "description": "A Noonan syndrome characterized by hypertrophic obstructive cardiomyopathy and that has_material_basis_in an autosomal recessive inheritance.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060580", 
        "name": "Noonan syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/605275", 
            "id": "605275", 
            "database": "MIM"
        }
    ]
}