{
    "disease_id": "DOID:0111567", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "grand Kaine fulling syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "RVCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "hereditary vascular retinopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "retinal vasculopathy and cerebral leukoencephalopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "CRV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "vasculopathy, retinal, with cerebral leukodystrophy; RVCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "RVCL-S"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "cerebroretinal vasculopathy, hereditary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "HVR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "grand-Kaine-fulling syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "autosomal dominant retinal vasculopathy with cerebral leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "cerebroretinal vasculopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "ADRVCL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008641", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008641", 
            "name": "vasculopathy, retinal, with cerebral leukodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "retinal vasculopathy and cerebral leukoencephalopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "CRV"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "RVCL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "RVCL-S"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "hereditary cerebroretinal vasculopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111567", 
            "name": "retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111567", 
        "description": "A vascular disease characterized by adult onset of microvascular endotheliopathy resulting in central nervous system degeneration with progressive loss of vision, stroke, motor impairment, and cognitive decline that has_material_basis_in heterozygous mutation in TREX1 on chromosome 3p21.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111567", 
        "name": "retinal vasculopathy with cerebral leukodystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111567#disease-associations", 
            "id": "0111567", 
            "database": "Alliance of Genome Resources"
        }
    ]
}