{
    "disease_id": "DOID:0112192",
    "recommended_name": {
        "id": "DOID:0112192",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112192",
        "name": "tetraamelia syndrome 1",
        "description": "A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that has_material_basis_in homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32."
    },
    "synonyms": [
        {
            "id": "DOID:0112192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112192",
            "name": "TETAMS1",
            "description": ""
        },
        {
            "id": "DOID:0112192",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112192",
            "name": "tetra-amelia syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0060764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060764",
            "name": "tetraamelia syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0060764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060764",
            "name": "Tetra-amelia syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0060764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060764",
            "name": "tetraamelia syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0060764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060764",
            "name": "TETAMS1",
            "description": ""
        },
        {
            "id": "MONDO:0060764",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0060764",
            "name": "tetraamelia syndrome, autosomal recessive",
            "description": ""
        },
        {
            "id": "MIM:273395",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/273395",
            "name": "Tetraamelia syndrome 1",
            "description": "Tetraamelia syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112192"
    ],
    "unlinked_id_list": []
}