{
    "disease_id": "DOID:0080523", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "pigmentary orthochromatic leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "subcortical gliosis of Neumann"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "GPSC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy, hereditary diffuse, with spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "adult-onset leukodystrophy with neuroaxonal spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "hereditary diffuse leukoencephalopathy with spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "ALSP"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "POLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "neuroaxonal leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "HDLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "familial dementia, Neumann type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy with neuroaxonal spheroids, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "dementia, familial, Neumann type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy, hereditary diffuse, with spheroids; HDLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "familial progressive subcortical gliosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "gliosis, familial progressive subcortical"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy, diffuse hereditary, with spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "FPSG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "hereditary diffuse leukoencephalopathy with axonal spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "autosomal dominant leukoencephalopathy with neuroaxonal spheroids"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009096", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009096", 
            "name": "leukoencephalopathy, diffuse hereditary, with spheroids; HDLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080523", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080523", 
            "name": "hereditary diffuse leukoencephalopathy with spheroids"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080523", 
        "description": "A leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has_material_basis_in heterozygous mutation in the CSF1R gene on chromosome 5q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080523", 
        "name": "adult-onset leukoencephalopathy with axonal spheroids and pigmented glia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080523#disease-associations", 
            "id": "0080523", 
            "database": "Alliance of Genome Resources"
        }
    ]
}