{
    "disease_id": "DOID:0111518",
    "recommended_name": {
        "id": "DOID:0111518",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111518",
        "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5",
        "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the RRM2B gene on chromosome 8q22.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111518",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111518",
            "name": "autosomal dominant progressive external ophthalmoplegia 5",
            "description": ""
        },
        {
            "id": "DOID:0111518",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111518",
            "name": "PEOA5",
            "description": ""
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5",
            "description": "Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RRM2B gene."
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions",
            "description": ""
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B",
            "description": ""
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5",
            "description": ""
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5",
            "description": ""
        },
        {
            "id": "MONDO:0013117",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "name": "PEOA5",
            "description": ""
        },
        {
            "id": "MIM:613077",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613077",
            "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5",
            "description": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111518"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0111518",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111518",
            "categories": []
        },
        {
            "id": "MONDO:0013117",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013117",
            "categories": []
        },
        {
            "id": "MIM:613077",
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            "url": "https://www.omim.org/entry/613077",
            "categories": []
        }
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                }
            ],
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                    "type": "synonym"
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                    "type": "recommended"
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                },
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                    "name": "Rrm2b",
                    "type": "recommended"
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                },
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                    "id": "0111518",
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        },
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                    "name": "Homo sapiens",
                    "taxid": 9606,
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                    "id": "0111518",
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                    "name": "Dmel\\CG8975",
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                    "name": "Rnrs",
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                    "name": "anon-WO0118547.148",
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                    "id": "0111518",
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                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q9VL76-1",
            "uniprot_ac": "Q9VL76",
            "uniprot_id": "PEO1_DROME",
            "refseq_ac": "NP_609318",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Drosophila melanogaster",
                    "taxid": 7227,
                    "common_name": "Fruit fly",
                    "glygen_name": "Fruit fly",
                    "reference_species": "Drosophila melanogaster [7227]"
                }
            ],
            "protein_names": [
                {
                    "name": "Mitochondrial DNA helicase",
                    "type": "recommended"
                },
                {
                    "name": "5.6.2.3",
                    "type": "synonym"
                },
                {
                    "name": "CG5924-PA",
                    "type": "synonym"
                },
                {
                    "name": "Twinkle mtDNA helicase",
                    "type": "synonym"
                },
                {
                    "name": "Twinkle protein, mitochondrial",
                    "type": "synonym"
                },
                {
                    "name": "d-mtDNA helicase",
                    "type": "synonym"
                },
                {
                    "name": "mitochondrial DNA helicase",
                    "type": "synonym"
                },
                {
                    "name": "mtDNA-helicase-PA",
                    "type": "synonym"
                },
                {
                    "name": "twinkle helicase",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "mtDNA-helicase",
                    "type": "recommended"
                },
                {
                    "name": "CG5924",
                    "type": "synonym"
                },
                {
                    "name": "Dmel\\CG5924",
                    "type": "synonym"
                },
                {
                    "name": "Twinkle",
                    "type": "synonym"
                },
                {
                    "name": "mtDNA helicase",
                    "type": "synonym"
                },
                {
                    "name": "mtDNA-helicase",
                    "type": "synonym"
                },
                {
                    "name": "twk",
                    "type": "synonym"
                }
            ],
            "record_id": "Q9VL76-1",
            "evidence": [
                {
                    "id": "0111518",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111518"
                }
            ]
        },
        {
            "uniprot_canonical_ac": "Q96RR1-1",
            "uniprot_ac": "Q96RR1",
            "uniprot_id": "PEO1_HUMAN",
            "refseq_ac": "NP_001157284",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Twinkle mtDNA helicase",
                    "type": "recommended"
                },
                {
                    "name": "5.6.2.3",
                    "type": "synonym"
                },
                {
                    "name": "Progressive external ophthalmoplegia 1 protein",
                    "type": "synonym"
                },
                {
                    "name": "T7 gp4-like protein with intramitochondrial nucleoid localization",
                    "type": "synonym"
                },
                {
                    "name": "T7 helicase-related protein with intramitochondrial nucleoid localization",
                    "type": "synonym"
                },
                {
                    "name": "T7-like mitochondrial DNA helicase",
                    "type": "synonym"
                },
                {
                    "name": "Twinkle protein, mitochondrial",
                    "type": "synonym"
                },
                {
                    "name": "ataxin 8",
                    "type": "synonym"
                },
                {
                    "name": "progressive external ophthalmoplegia 1 protein",
                    "type": "synonym"
                },
                {
                    "name": "twinkle mtDNA helicase isoform B",
                    "type": "synonym"
                },
                {
                    "name": "twinkle protein, mitochondrial",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "TWNK",
                    "type": "recommended"
                },
                {
                    "name": "ATXN8",
                    "type": "synonym"
                },
                {
                    "name": "C10orf2",
                    "type": "synonym"
                },
                {
                    "name": "IOSCA",
                    "type": "synonym"
                },
                {
                    "name": "MTDPS7",
                    "type": "synonym"
                },
                {
                    "name": "PEO1",
                    "type": "synonym"
                },
                {
                    "name": "PEOA3",
                    "type": "synonym"
                },
                {
                    "name": "PEO",
                    "type": "synonym"
                },
                {
                    "name": "PRLTS5",
                    "type": "synonym"
                },
                {
                    "name": "SANDO",
                    "type": "synonym"
                },
                {
                    "name": "SCA8",
                    "type": "synonym"
                },
                {
                    "name": "TWINL",
                    "type": "synonym"
                },
                {
                    "name": "TWNK",
                    "type": "synonym"
                }
            ],
            "record_id": "Q96RR1-1",
            "evidence": [
                {
                    "id": "0111518",
                    "database": "AGR",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111518"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0111518"
}