{
    "disease_id": "DOID:0070010", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013358", 
            "name": "Seckel syndrome 4; SCKL4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013358", 
            "name": "CENPJ Seckel syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013358", 
            "name": "Seckel syndrome type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013358", 
            "name": "Seckel syndrome caused by mutation in CENPJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013358", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013358", 
            "name": "SCKL4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070010", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070010", 
            "name": "SCKL4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070010", 
        "description": "A Seckel syndrome that has_material_basis_in homozygous mutation in the CENPJ gene on chromosome 13q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070010", 
        "name": "Seckel syndrome 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613676", 
            "id": "613676", 
            "database": "MIM"
        }
    ]
}