{
    "disease_id": "DOID:0060285",
    "recommended_name": {
        "id": "DOID:0060285",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060285",
        "name": "parietal foramina",
        "description": "An inherited neural tube defect that is characterized by enlarged openings in the parietal bones of the skull, has_material_basis_in mutation in the ALX4 gene or MSX2 gene."
    },
    "synonyms": [
        {
            "id": "DOID:0060285",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060285",
            "name": "Caitlin marks",
            "description": ""
        },
        {
            "id": "DOID:0060285",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060285",
            "name": "enlarged parietal foramina",
            "description": ""
        },
        {
            "id": "DOID:0060285",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060285",
            "name": "hereditary cranium bifidum",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "parietal foramina 1",
            "description": "Any parietal foramina in which the cause of the disease is a mutation in the MSX2 gene."
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "MSX2 parietal foramina",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "parietal foramina 1",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "parietal foramina caused by mutation in MSX2",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "PFM",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "PFM1",
            "description": ""
        },
        {
            "id": "MONDO:0008197",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008197",
            "name": "parietal foramina",
            "description": ""
        },
        {
            "id": "MONDO:0012302",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012302",
            "name": "parietal foramina 3",
            "description": ""
        },
        {
            "id": "MONDO:0012302",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012302",
            "name": "PFM3",
            "description": ""
        },
        {
            "id": "MONDO:0012302",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012302",
            "name": "parietal foramina 3",
            "description": ""
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "parietal foramina 2",
            "description": "Any parietal foramina in which the cause of the disease is a mutation in the ALX4 gene."
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "ALX4 parietal foramina",
            "description": ""
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "parietal foramina 2",
            "description": ""
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "parietal foramina caused by mutation in ALX4",
            "description": ""
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "parietal foramina type 2",
            "description": ""
        },
        {
            "id": "MONDO:0012309",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012309",
            "name": "PFM2",
            "description": ""
        },
        {
            "id": "MIM:168500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/168500",
            "name": "Parietal foramina 1",
            "description": "Parietal foramina 1"
        },
        {
            "id": "MIM:609597",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609597",
            "name": "Parietal foramina 2",
            "description": "Parietal foramina 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060285"
    ],
    "unlinked_id_list": []
}