{
    "disease_id": "DOID:0070329", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "mitochondrial DNA depletion syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "mitochondrial DNA depletion syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "myoneurogastrointestinal encephalopathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "mitochondrial DNA depletion syndrome 1 (MNGIE type)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "Polip syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "mitochondrial neurogastrointestinal encephalopathy syndrome, tymp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "Mngie, tymp-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "MTDPS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011283", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011283", 
            "name": "mitochondrial DNA depletion syndrome 1 (MNGIE type); MTDPS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070329", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070329", 
            "name": "mtDNA depletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070329", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070329", 
        "name": "mitochondrial DNA depletion syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070329#disease-associations", 
            "id": "0070329", 
            "database": "Alliance of Genome Resources"
        }
    ]
}