{
    "disease_id": "DOID:0050454", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "periventricular nodular heterotopia 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "periventricular nodular heterotopia type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "ERMARD periventricular nodular heterotopia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "periventricular nodular heterotopia caused by mutation in ERMARD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "PVNH6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014240", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014240", 
            "name": "periventricular nodular heterotopia 6; PVNH6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050454", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050454", 
            "name": "periventricular heterotopia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050454", 
        "description": "A congenital nervous system abnormality characterized by non proper migration of neurons during the early development of the fetal brain.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050454", 
        "name": "periventricular nodular heterotopia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050454#disease-associations", 
            "id": "0050454", 
            "database": "Alliance of Genome Resources"
        }
    ]
}