{
    "disease_id": "DOID:0050469", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009026", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009026", 
            "name": "Costello syndrome; CSTLO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009026", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009026", 
            "name": "CSTLO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009026", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009026", 
            "name": "FCS syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009026", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009026", 
            "name": "faciocutaneoskeletal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009026", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009026", 
            "name": "myopathy, congenital, with excess of muscle spindles"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050469", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050469", 
            "name": "FCS SYNDROME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050469", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050469", 
            "name": "Faciocutaneoskeletal Syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050469", 
        "description": "A RASopathy characterized by craniofacial dysmorphology, cardiac defects, mild mental retardation, and high birth weight followed by a failure to thrive and developmental delays.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050469", 
        "name": "Costello syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050469#disease-associations", 
            "id": "0050469", 
            "database": "Alliance of Genome Resources"
        }
    ]
}