{
    "disease_id": "DOID:0060786", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "Pelizaeus-Merzbacher disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "leukodystrophy, sudanophilic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "leukodystrophy, hypomyelinating, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "sudanophilic leukodystrophy, Paelizeus-Merzbacher type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "Pelizaeus Merzbacher brain sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "hypomyelinating leukodystrophy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "Pelizaeus-Merzbacher brain sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "Pelizaeus-Merzbacher disease; PMD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "HLD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "diffuse familial brain sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "Pelizaeus Merzbacher disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010714", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010714", 
            "name": "PMD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060786", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060786", 
            "name": "HLD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060786", 
        "description": "A leukodystrophy characterized by T2 hyperintensity and T1 iso- or hyperintensity of affected white matter in the central nervous system.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060786", 
        "name": "hypomyelinating leukodystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060786#disease-associations", 
            "id": "0060786", 
            "database": "Alliance of Genome Resources"
        }
    ]
}