{
    "disease_id": "DOID:0080488",
    "recommended_name": {
        "id": "DOID:0080488",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080488",
        "name": "mucolipidosis",
        "description": "A lipid storage disease that is characterized by increased storage of carbohydrates and lipids."
    },
    "synonyms": [
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis type 2",
            "description": "A rare lysosomal storage disease, and the severe, early onset form of sialidosis characterized by a progressively severe mucopolysaccharidosis-like phenotype (coarse facies, dysostosis multiplex, hepatosplenomegaly), macular cherry-red spots as well as psychomotor and developmental delay. ST-2 displays a broad spectrum of clinical severity with antenatal/congenital, infantile and juvenile presentations."
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "NEU1 sialidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "dysmorphic sialidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "dysmorphic sialidosis with renal involvement",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "infantile dysmorphic sialidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "mucolipidosis I",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "nephrosialidosis",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis caused by mutation in NEU1",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis type II",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "ML1",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "NEU 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "mucolipidosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009738",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009738",
            "name": "sialidosis, type II",
            "description": ""
        },
        {
            "id": "MIM:256550",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256550",
            "name": "Sialidosis",
            "description": "Sialidosis"
        }
    ],
    "children": [
        {
            "id": "DOID:0080070",
            "label": "mucolipidosis II alpha/beta",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080071",
            "label": "mucolipidosis III alpha/beta",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080490",
            "label": "mucolipidosis type IV",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080678",
            "label": "mucolipidosis III gamma",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:3343",
            "label": "glycoproteinosis",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0080071",
        "DOID:0080490",
        "DOID:0080070",
        "DOID:0080678",
        "DOID:3343",
        "DOID:0080488"
    ],
    "unlinked_id_list": []
}