{
    "disease_id": "DOID:0110972", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "brachydactyly, type E1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "brachydactyly type E caused by mutation in HOXD13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "HOXD13 brachydactyly type E"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "brachydactyly, type E1; BDE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "BDE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007223", 
            "name": "brachydactyly, type E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110972", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110972", 
            "name": "BDE1"
        }, 
        {
            "url": "https://www.omim.org/entry/113300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:113300", 
            "name": "Brachydactyly E1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110972", 
        "description": "A brachydactyly characterized by shortening of the fingers,mainly in the metacarpals and metatarsals, that has_material_basis_in heterozygous mutation in the HOXD13 gene on chromosome 2q31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110972", 
        "name": "brachydactyly type E1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/113300", 
            "id": "113300", 
            "database": "MIM"
        }
    ]
}