{
    "disease_id": "DOID:0111199",
    "recommended_name": {
        "id": "DOID:0111199",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111199",
        "name": "autosomal dominant distal hereditary motor neuronopathy 7",
        "description": "An autosomal dominant distal hereditary motor neuronopathy that is characterized by slowly progressive distal atrophy and weakness affecting first the upper limbs and later the lower limbs and vocal cord paresis and that has_material_basis_in heterozygous mutation in the SLC5A7 gene on 2q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "DHMN7A",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "DHMNVPy",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "HMN VIIA",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "HMN7A",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "Harper-Young myopath",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "dHMN7",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "distal hereditary motor neuropathy type VIIA",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "distal spinal muscular atrophy with vocal cord paralysis",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "distal spinal muscular atrophy with vocal cord paralysis type 7A",
            "description": ""
        },
        {
            "id": "DOID:0111199",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111199",
            "name": "distal hereditary motor neuronopathy type 7",
            "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": "SLC5A7 neuronopathy, distal hereditary motor",
            "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": "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": "neuronopathy, distal hereditary motor, type VIIA",
            "description": ""
        },
        {
            "id": "MIM:158580",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/158580",
            "name": "Neuronopathy, distal hereditary motor, autosomal dominant 7",
            "description": "Neuronopathy, distal hereditary motor, autosomal dominant 7"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111199"
    ],
    "unlinked_id_list": []
}