{
    "disease_id": "DOID:0111210",
    "recommended_name": {
        "id": "DOID:0111210",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111210",
        "name": "distal hereditary motor neuronopathy type 2D",
        "description": "A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in FBXO38 on 5q32."
    },
    "synonyms": [
        {
            "id": "DOID:0111210",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111210",
            "name": "HMN IID",
            "description": ""
        },
        {
            "id": "DOID:0111210",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111210",
            "name": "HMN2D",
            "description": ""
        },
        {
            "id": "DOID:0111210",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111210",
            "name": "distal hereditary motor neuropathy type IID",
            "description": ""
        },
        {
            "id": "DOID:0111210",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111210",
            "name": "distal spinal muscular atrophy with calf predominance",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "neuronopathy, distal hereditary motor, type 2D",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the FBXO38 gene."
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "HMN2D",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "neuropathy, distal hereditary motor, type 2D",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "neuronopathy, distal hereditary motor, type IID; HMN2D",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "neuronopathy, distal hereditary motor caused by mutation in FBXO38",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "spinal muscular atrophy, distal, autosomal dominant, calf-predominant",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "neuronopathy, distal hereditary motor, type IID",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "FBXO38 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0014259",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014259",
            "name": "HMN 2D",
            "description": ""
        },
        {
            "id": "MIM:615575",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615575",
            "name": "Neuronopathy, distal hereditary motor, 2D",
            "description": "Neuronopathy, distal hereditary motor, 2D"
        }
    ]
}