{
    "disease_id": "DOID:0111205",
    "recommended_name": {
        "id": "DOID:0111205",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111205",
        "name": "autosomal dominant distal hereditary motor neuronopathy 12",
        "description": "An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the REEP1 gene on 2p11.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111205",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111205",
            "name": "distal HMN VB",
            "description": ""
        },
        {
            "id": "DOID:0111205",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111205",
            "name": "distal spinal muscular atrophy type VB",
            "description": ""
        },
        {
            "id": "DOID:0111205",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111205",
            "name": "distal hereditary motor neuronopathy type 5B",
            "description": ""
        },
        {
            "id": "MONDO:0013884",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013884",
            "name": "neuronopathy, distal hereditary motor, type 5B",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the REEP1 gene."
        },
        {
            "id": "MONDO:0013884",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013884",
            "name": "REEP1 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0013884",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013884",
            "name": "neuronopathy, distal hereditary motor caused by mutation in REEP1",
            "description": ""
        },
        {
            "id": "MONDO:0013884",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013884",
            "name": "HMN5B",
            "description": ""
        },
        {
            "id": "MONDO:0013884",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013884",
            "name": "neuronopathy, distal hereditary motor, type VB",
            "description": ""
        },
        {
            "id": "MIM:614751",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614751",
            "name": "Neuronopathy, distal hereditary motor, autosomal dominant 12",
            "description": "Neuronopathy, distal hereditary motor, autosomal dominant 12"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111205"
    ],
    "unlinked_id_list": []
}