{
    "disease_id": "DOID:0111211",
    "recommended_name": {
        "id": "DOID:0111211",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111211",
        "name": "distal spinal muscular atrophy type 3",
        "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and wasting with variable severity that has_material_basis_in homozygous mutation in a 2.6-cM region of chromosome 11q13.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111211",
            "name": "distal hereditary motor neuropathy type 3 and type 4",
            "description": ""
        },
        {
            "id": "DOID:0111211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111211",
            "name": "dHMN3 and dHMN4",
            "description": ""
        },
        {
            "id": "DOID:0111211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111211",
            "name": "dSMA3",
            "description": ""
        },
        {
            "id": "DOID:0111211",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111211",
            "name": "autosomal recessive distal spinal muscular atrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "distal spinal muscular atrophy type 3",
            "description": "Distal spinal muscular atrophy type 3 is a rare neuromuscular disease characterized by progressive muscular weakness and atrophy predominantly affecting distal parts of limbs, later involvement of proximal and trunk muscles with marked hyperlordosis and late diaphragmatic dysfunction."
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "dHMN3 and dHMN4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "dHMN4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "dHMN3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "HMN 4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "dSMA3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "HMN 3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "spinal muscular atrophy, chronic distal, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "spinal muscular atrophy, distal, autosomal recessive, 3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "autosomal recessive distal spinal muscular atrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "neuronopathy, distal hereditary motor, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "distal hereditary motor neuropathy type 3 and type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "neuropathy, distal hereditary motor, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0011771",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011771",
            "name": "neuronopathy, distal hereditary motor, type 3",
            "description": ""
        }
    ]
}