{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "parietal foramina 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "PFM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "foramina parietalia permagna"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "parietal foramina 1; PFM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "cranium bifidum, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "PFM"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "catlin Marks"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "parietal foramina caused by mutation in MSX2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "cranium bifidum occultum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "MSX2 parietal foramina"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "parietal foramina, symmetric"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008197", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008197", 
            "name": "parietal foramina; PFM"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060285", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060285", 
            "name": "Caitlin marks"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060285", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060285", 
            "name": "enlarged parietal foramina"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060285", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060285", 
            "name": "hereditary cranium bifidum"
        }, 
        {
            "url": "https://www.omim.org/entry/168500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:168500", 
            "name": "Parietal foramina 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060285", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060285", 
        "name": "parietal foramina"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/168500", 
            "id": "168500", 
            "database": "MIM"
        }
    ]
}