{
    "disease_id": "DOID:0070009",
    "recommended_name": {
        "id": "DOID:0070009",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070009",
        "name": "Seckel syndrome 8",
        "description": "A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21."
    },
    "synonyms": [
        {
            "id": "DOID:0070009",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070009",
            "name": "SCKL8",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "Seckel syndrome 8",
            "description": "Any Seckel syndrome in which the cause of the disease is a mutation in the DNA2 gene."
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "Seckel syndrome caused by mutation in DNA2",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "Seckel syndrome 8; SCKL8",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "Seckel syndrome type 8",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "SCKL8",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "DNA2 Seckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014350",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014350",
            "name": "Seckel syndrome 8",
            "description": ""
        },
        {
            "id": "MIM:615807",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615807",
            "name": "Seckel syndrome 8",
            "description": "Seckel syndrome 8"
        }
    ]
}