{
    "disease_id": "DOID:0112313",
    "recommended_name": {
        "id": "DOID:0112313",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112313",
        "name": "brain small vessel disease",
        "description": "A brain disease characterized by abnormalities in the small blood vessels in the brain."
    },
    "synonyms": [
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease 1 with or without ocular anomalies",
            "description": "Any porencephaly in which the cause of the disease is a mutation in the COL4A1 gene."
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "ADT1P",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "BSVD",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "BSVD1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "COL4A1 porencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "COL4A1-related brain small vessel disease with haemorrhage",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "COL4A1-related brain small vessel disease with hemorrhage",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "COL4A1-related familial vascular leukoencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "T1P",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease with Axenfeld-Riegar anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease with axenfeld-rieger anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease with haemorrhage",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease with hemorrhage",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "brain small vessel disease with or without ocular anomalies",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "hemiplegia, infantile, with porencephaly",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "infantile hemiparesis",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "leukoencephalopathy with axenfeld-rieger anomaly",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "porencephaly 1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "porencephaly caused by mutation in COL4A1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "porencephaly type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "POREN1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "hemiplegia, infantile, with porencephaly porencephaly, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008289",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008289",
            "name": "porencephaly, type 1, autosomal dominant",
            "description": ""
        },
        {
            "id": "MIM:175780",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/175780",
            "name": "Brain small vessel disease 1 with or without ocular anomalies",
            "description": "Brain small vessel disease 1 with or without ocular anomalies"
        }
    ],
    "children": [
        {
            "id": "DOID:0090125",
            "label": "brain small vessel disease 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112315",
            "label": "brain small vessel disease 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0112314",
            "label": "brain small vessel disease 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0112313",
        "DOID:0090125",
        "DOID:0112315",
        "DOID:0112314"
    ],
    "unlinked_id_list": []
}