{
    "disease_id": "DOID:0111201",
    "recommended_name": {
        "id": "DOID:0111201",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111201",
        "name": "distal hereditary motor neuronopathy type 7A",
        "description": "A distal hereditary motor neuropathy type 7 characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis that has_material_basis_in heterozygous mutation in SLC5A7 on 2q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "DHMN7A",
            "description": ""
        },
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "HMN VIIA",
            "description": ""
        },
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "HMN7A",
            "description": ""
        },
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "Harper-Young myopath",
            "description": ""
        },
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "distal hereditary motor neuropathy type VIIA",
            "description": ""
        },
        {
            "id": "DOID:0111201",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111201",
            "name": "distal spinal muscular atrophy with vocal cord paralysis type 7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "neuronopathy, distal hereditary motor, type 7A",
            "description": "Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the SLC5A7 gene."
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "neuronopathy, distal hereditary motor, type VIIA",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "spinal muscular atrophy, distal, with vocal cord paralysis",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "Harper-Young myopathy",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "neuronopathy, distal hereditary motor, type VIIA; HMN7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "SLC5A7 neuronopathy, distal hereditary motor",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "HMN 7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "Dhmn7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "Dhmnvp",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "HMN7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "neuropathy, distal hereditary motor, type 7A",
            "description": ""
        },
        {
            "id": "MONDO:0008024",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008024",
            "name": "neuronopathy, distal hereditary motor caused by mutation in SLC5A7",
            "description": ""
        },
        {
            "id": "MIM:158580",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/158580",
            "name": "Neuronopathy, distal hereditary motor, 7A",
            "description": "Neuronopathy, distal hereditary motor, 7A"
        }
    ]
}