{
    "disease_id": "DOID:0060790",
    "recommended_name": {
        "id": "DOID:0060790",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060790",
        "name": "hypomyelinating leukodystrophy 3",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060790",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060790",
            "name": "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation",
            "description": ""
        },
        {
            "id": "DOID:0060790",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060790",
            "name": "HLD3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "hypomyelinating leukodystrophy 3",
            "description": "Any leukodystrophy in which the cause of the disease is a mutation in the AIMP1 gene."
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "AIMP1 leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "HLD3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "Pelizaeus-Merzbacher-like disease due to AIMP1 mutation",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "hypomyelinating leukodystrophy 3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "hypomyelinating leukodystrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "leukodystrophy caused by mutation in AIMP1",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "leukodystrophy, hypomyelinating, type 3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "leukodystrophy, hypomyelinating 3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "leukodystrophy, hypomyelinating, 3",
            "description": ""
        },
        {
            "id": "MONDO:0009843",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009843",
            "name": "perinatal Sudanophilic leukodystrophy",
            "description": ""
        },
        {
            "id": "MIM:260600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/260600",
            "name": "Leukodystrophy, hypomyelinating, 3",
            "description": "Leukodystrophy, hypomyelinating, 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060790"
    ],
    "unlinked_id_list": []
}