{
    "disease_id": "DOID:0111153",
    "recommended_name": {
        "id": "DOID:0111153",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111153",
        "name": "congenital mirror movement disorder",
        "description": "A movement disease characterized by involuntary movements of one side of the body that mirror intentional movements on the opposite side primarily involving the upper limbs."
    },
    "synonyms": [
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "familial congenital controlateral synkinesia",
            "description": ""
        },
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "familial congenital mirror movements",
            "description": ""
        },
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "hereditary congenital controlateral synkinesia",
            "description": ""
        },
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "hereditary congenital mirror movements",
            "description": ""
        },
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "isolated congenital controlateral synkinesia",
            "description": ""
        },
        {
            "id": "DOID:0111153",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "name": "isolated congenital mirror movements",
            "description": ""
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "mirror movements 1",
            "description": "Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene."
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "DCC familial congenital mirror movements",
            "description": ""
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "familial congenital mirror movements caused by mutation in DCC",
            "description": ""
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "mirror movements 1",
            "description": ""
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "mirror movements type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008002",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "name": "MRMV1",
            "description": ""
        },
        {
            "id": "MIM:157600",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/157600",
            "name": "Mirror movements 1",
            "description": "Mirror movements 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0070636",
            "label": "mirror movements 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070637",
            "label": "mirror movements 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070638",
            "label": "mirror movements 4",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0070639",
            "label": "mirror movements 3",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0070639",
        "DOID:0070637",
        "DOID:0070638",
        "DOID:0111153",
        "DOID:0070636"
    ],
    "unlinked_id_list": [],
    "crossref": [
        {
            "id": "DOID:0111153",
            "database": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111153",
            "categories": []
        },
        {
            "id": "MONDO:0008002",
            "database": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008002",
            "categories": []
        },
        {
            "id": "MIM:157600",
            "database": "MIM",
            "url": "https://www.omim.org/entry/157600",
            "categories": []
        }
    ],
    "proteins": [
        {
            "uniprot_canonical_ac": "P43146-1",
            "uniprot_ac": "P43146",
            "uniprot_id": "DCC_HUMAN",
            "refseq_ac": "NP_005206",
            "glycoprotein": "yes",
            "species": [
                {
                    "name": "Homo sapiens",
                    "taxid": 9606,
                    "common_name": "Human",
                    "glygen_name": "Human",
                    "reference_species": "Homo sapiens [9606]"
                }
            ],
            "protein_names": [
                {
                    "name": "Netrin receptor DCC",
                    "type": "recommended"
                },
                {
                    "name": "Colorectal cancer suppressor",
                    "type": "synonym"
                },
                {
                    "name": "Immunoglobulin superfamily DCC subclass member 1",
                    "type": "synonym"
                },
                {
                    "name": "Tumor suppressor protein DCC",
                    "type": "synonym"
                },
                {
                    "name": "colorectal cancer suppressor",
                    "type": "synonym"
                },
                {
                    "name": "deleted in colorectal carcinoma",
                    "type": "synonym"
                },
                {
                    "name": "immunoglobulin superfamily DCC subclass member 1",
                    "type": "synonym"
                },
                {
                    "name": "netrin receptor DCC",
                    "type": "synonym"
                },
                {
                    "name": "putative colorectal tumor suppressor",
                    "type": "synonym"
                },
                {
                    "name": "tumor suppressor protein DCC",
                    "type": "synonym"
                }
            ],
            "gene_names": [
                {
                    "name": "DCC",
                    "type": "recommended"
                },
                {
                    "name": "CRC18",
                    "type": "synonym"
                },
                {
                    "name": "CRCR1",
                    "type": "synonym"
                },
                {
                    "name": "DCC",
                    "type": "synonym"
                },
                {
                    "name": "HGPPS2",
                    "type": "synonym"
                },
                {
                    "name": "IGDCC1",
                    "type": "synonym"
                },
                {
                    "name": "MRMV1",
                    "type": "synonym"
                },
                {
                    "name": "NTN1R1",
                    "type": "synonym"
                }
            ],
            "record_id": "P43146-1",
            "evidence": [
                {
                    "id": "157600",
                    "database": "MIM",
                    "url": "https://www.omim.org/entry/157600"
                }
            ]
        }
    ],
    "glycans": [],
    "biomarkers": [],
    "association_flag": "1000",
    "record_id": "doid.0111153"
}