{
    "disease_id": "DOID:0070744",
    "recommended_name": {
        "id": "DOID:0070744",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070744",
        "name": "early childhood-onset progressive leukodystrophy",
        "description": "A leukodystrophy characterized by infantile onset of stagnation and regression of motor and language development progressing to complete lack of communication and purposeful movement that has_material_basis_in homozygous mutation in the ACER3 gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0070744",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070744",
            "name": "PLDECO",
            "description": ""
        },
        {
            "id": "DOID:0070744",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070744",
            "name": "alkaline ceramidase 3 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0044718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044718",
            "name": "alkaline ceramidase 3 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0044718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044718",
            "name": "ACER3-related early childhood-onset progressive leukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0044718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044718",
            "name": "leukodystrophy due to alkaline ceramidase 3 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0044718",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0044718",
            "name": "PLDECO",
            "description": ""
        },
        {
            "id": "MIM:617762",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617762",
            "name": "Leukodystrophy, progressive, early childhood-onset",
            "description": "Leukodystrophy, progressive, early childhood-onset"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070744"
    ],
    "unlinked_id_list": []
}
