{
    "disease_id": "DOID:0060785", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "leukodystrophy, demyelinating, ADULT-onset, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "autosomal dominant adult-onset demyelinating leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "multiple sclerosis-like disorder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "adult-onset autosomal dominant leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "ADLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "autosomal dominant leukodystrophy with autonomic disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008215", 
            "name": "leukodystrophy, demyelinating, ADULT-onset, autosomal dominant; ADLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060785", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060785", 
            "name": "ADLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060785", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060785", 
            "name": "adult-onset autosomal dominant leukodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060785", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060785", 
            "name": "autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060785", 
        "description": "A leukodystrophy characterized by onset in the 4th or 5th decade of life of autonomic abnormalities, pyramidal and cerebellar dysfunction, and symmetric demyelination of the CNS that has_material_basis_in heterozygous tandem genomic duplication resulting in an extra copy of the LMNB1 gene on chromosome 5q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060785", 
        "name": "adult-onset autosomal dominant demyelinating leukodystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060785#disease-associations", 
            "id": "0060785", 
            "database": "Alliance of Genome Resources"
        }
    ]
}