{
    "disease_id": "DOID:0060790", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "leukodystrophy, hypomyelinating, 3; HLD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "leukodystrophy caused by mutation in AIMP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "HLD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "leukodystrophy, hypomyelinating, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "hypomyelinating leukodystrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "perinatal Sudanophilic leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "leukodystrophy, hypomyelinating 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "AIMP1 leukodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009843", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009843", 
            "name": "leukodystrophy, hypomyelinating, 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060790", 
            "name": "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060790", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060790", 
            "name": "HLD3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060790", 
        "description": "A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of early infantile onset of global developmental delay, lack of development, lack of speech acquisition, and peripheral spasticity associated with decreased myelination in the central nervous system that has_material_basis_in homozygous mutation in the AIMP1 gene on chromosome 4q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060790", 
        "name": "hypomyelinating leukodystrophy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060790#disease-associations", 
            "id": "0060790", 
            "database": "Alliance of Genome Resources"
        }
    ]
}