{
    "disease_id": "DOID:0111161",
    "recommended_name": {
        "id": "DOID:0111161",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111161",
        "name": "Crouzon syndrome-acanthosis nigricans syndrome",
        "description": "A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has_material_basis_in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16."
    },
    "synonyms": [
        {
            "id": "DOID:0111161",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111161",
            "name": "CAN",
            "description": ""
        },
        {
            "id": "DOID:0111161",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111161",
            "name": "Crouzon-dermoskeletal syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111161",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111161",
            "name": "Crouzonodermoskeletal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Crouzon syndrome-acanthosis nigricans syndrome",
            "description": "Crouzon syndrome with acanthosis nigricans (CAN) is a very rare, clinically heterogeneous form of faciocraniostenosis with Crouzon-like features and premature synostosis of cranial sutures (Crouzon disease, see this term), associated with acanthosis nigricans (AN; see this term)."
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Crouzon syndrome with acanthosis nigricans; can",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Chronic kidney allograft nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "chronic allograft nephropathy",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Crouzon syndrome with acanthosis nigricans",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Crouzon-dermoskeletal syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "CAN",
            "description": ""
        },
        {
            "id": "MONDO:0012833",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012833",
            "name": "Crouzonodermoskeletal syndrome",
            "description": ""
        },
        {
            "id": "MIM:612247",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612247",
            "name": "Crouzon syndrome with acanthosis nigricans",
            "description": "Crouzon syndrome with acanthosis nigricans"
        }
    ]
}