{
    "disease_id": "DOID:0081425",
    "recommended_name": {
        "id": "DOID:0081425",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081425",
        "name": "autosomal recessive distal hereditary motor neuronopathy 6",
        "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by onset of distal muscle weakness in early infancy and that has_material_basis_in homozygous mutation in the REEP1 gene on chromosome 2p11."
    },
    "synonyms": [
        {
            "id": "MONDO:0859279",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859279",
            "name": "spinal muscular atrophy, distal, autosomal recessive, 6",
            "description": ""
        },
        {
            "id": "MONDO:0859279",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0859279",
            "name": "DSMA6",
            "description": ""
        },
        {
            "id": "MIM:620011",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/620011",
            "name": "Neuronopathy, distal hereditary motor, autosomal recessive 6",
            "description": "Neuronopathy, distal hereditary motor, autosomal recessive 6"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081425"
    ],
    "unlinked_id_list": []
}