{
    "disease_id": "DOID:0070007",
    "recommended_name": {
        "id": "DOID:0070007",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070007",
        "name": "Seckel syndrome 1",
        "description": "A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23."
    },
    "synonyms": [
        {
            "id": "DOID:0070007",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070007",
            "name": "SCKL1",
            "description": ""
        },
        {
            "id": "DOID:0070007",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070007",
            "name": "microcephalic primordial dwarfism I",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 1",
            "description": "Any Seckel syndrome in which the cause of the disease is a mutation in the ATR gene."
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "ATR Seckel syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "SCKL1",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome 3",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome caused by mutation in ATR",
            "description": ""
        },
        {
            "id": "MONDO:0008869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008869",
            "name": "Seckel syndrome type 1",
            "description": ""
        },
        {
            "id": "MIM:210600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/210600",
            "name": "Seckel syndrome 1",
            "description": "Seckel syndrome 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070007"
    ],
    "unlinked_id_list": []
}