{
    "disease_id": "DOID:0070329",
    "recommended_name": {
        "id": "DOID:0070329",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070329",
        "name": "mitochondrial DNA depletion syndrome",
        "description": "A mitochondrial metabolism disease that is characterized by significant reduction in mitochondrial DNA in affected tissues, resulting in impaired mtDNA-encoded protein synthesis and energy production in the affected tissues and organs."
    },
    "synonyms": [
        {
            "id": "DOID:0070329",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070329",
            "name": "mtDNA depletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "mitochondrial DNA depletion syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "mitochondrial DNA depletion syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "myoneurogastrointestinal encephalopathy syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "mitochondrial DNA depletion syndrome 1 (MNGIE type)",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "Polip syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "mitochondrial neurogastrointestinal encephalopathy syndrome, tymp-related",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "Mngie, tymp-related",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "MTDPS1",
            "description": ""
        },
        {
            "id": "MONDO:0011283",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011283",
            "name": "mitochondrial DNA depletion syndrome 1 (MNGIE type); MTDPS1",
            "description": ""
        },
        {
            "id": "MIM:603041",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603041",
            "name": "Mitochondrial DNA depletion syndrome 1, MNGIE type",
            "description": "Mitochondrial DNA depletion syndrome 1, MNGIE type"
        }
    ]
}