{
    "disease_id": "DOID:0080125",
    "recommended_name": {
        "id": "DOID:0080125",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080125",
        "name": "mitochondrial DNA depletion syndrome 6",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0080125",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080125",
            "name": "Navajo neurohepatopathy",
            "description": ""
        },
        {
            "id": "DOID:0080125",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080125",
            "name": "MPV17-related hepatocerebral mitochondrial DNA depletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "mitochondrial DNA depletion syndrome 6 (hepatocerebral type)",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "Navajo neurohepatopathy",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "Navajo neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "mitochondrial DNA depletion syndrome 6 (hepatocerebral type)",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "MPV17-related hepatocerebral mitochondrial DNA depletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "MTDPS6",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "NN",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "Navajo familial neurogenic arthropathy",
            "description": ""
        },
        {
            "id": "MONDO:0009747",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009747",
            "name": "mitochondrial DNA depletion syndrome 6",
            "description": ""
        },
        {
            "id": "MIM:256810",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/256810",
            "name": "Mitochondrial DNA depletion syndrome 6",
            "description": "Mitochondrial DNA depletion syndrome 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080125"
    ],
    "unlinked_id_list": []
}