{
    "disease_id": "DOID:0080963",
    "recommended_name": {
        "id": "DOID:0080963",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080963",
        "name": "anauxetic dysplasia 3",
        "description": "A spondyloepimetaphyseal dysplasia that is characterized by severe short stature, brachydactyly, skin laxity, joint hypermobility, and joint dislocations and that has_material_basis_in homozygous mutation in the NEPRO gene on chromosome 3q13."
    },
    "synonyms": [
        {
            "id": "MONDO:0030019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030019",
            "name": "anauxetic dysplasia 3",
            "description": ""
        },
        {
            "id": "MONDO:0030019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030019",
            "name": "ANAUXETIC DYSPLASIA 3",
            "description": ""
        },
        {
            "id": "MONDO:0030019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030019",
            "name": "ANXD3",
            "description": ""
        },
        {
            "id": "MONDO:0030019",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030019",
            "name": "anauxetic dysplasia 3",
            "description": ""
        },
        {
            "id": "MIM:618853",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618853",
            "name": "Anauxetic dysplasia 3",
            "description": "Anauxetic dysplasia 3"
        }
    ]
}