{
    "disease_id": "DOID:0080125", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "Navajo neurohepatopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "MPV17-related hepatocerebral mitochondrial DNA depletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "NN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "Navajo familial neurogenic arthropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "mitochondrial DNA depletion syndrome 6 (hepatocerebral type); MTDPS6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "mitochondrial DNA depletion syndrome 6 (hepatocerebral type)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "Navajo neuropathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009747", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009747", 
            "name": "MTDPS6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080125", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080125", 
            "name": "Navajo neurohepatopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080125", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080125", 
            "name": "MPV17-related hepatocerebral mitochondrial DNA depletion syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080125", 
        "description": "A mitochondrial DNA depletion syndrome that is characterized by infantile onset of progressive liver failure, often leading to death in the first year of life, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the mitochondrial inner membrane protein MPV17 gene on chromosome 2p23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080125", 
        "name": "mitochondrial DNA depletion syndrome 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080125#disease-associations", 
            "id": "0080125", 
            "database": "Alliance of Genome Resources"
        }
    ]
}