{
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111601", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111601", 
            "name": "DA2B2"
        }, 
        {
            "url": "https://www.omim.org/entry/618435", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:618435", 
            "name": "Arthrogryposis, distal, 2B2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111601", 
        "description": "A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in TNNT3 on chromosome 11p15.5.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111601", 
        "name": "distal arthrogryposis type 2B2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/618435", 
            "id": "618435", 
            "database": "MIM"
        }
    ]
}