{
    "disease_id": "DOID:13137",
    "recommended_name": {
        "id": "DOID:13137",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13137",
        "name": "Werdnig-Hoffmann disease",
        "description": "A childhood spinal muscular atrophy that is a severe form and is characterized by muscle weakness onset from birth to six months of age, the inability to sit unassisted."
    },
    "synonyms": [
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "HMN (Hereditary motor Neuropathy) Proximal type I",
            "description": ""
        },
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "SMA1",
            "description": ""
        },
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "Spinal muscular atrophy 1",
            "description": ""
        },
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "hereditary motor neuropathy proximal type I",
            "description": ""
        },
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "infantile muscular atrophy",
            "description": ""
        },
        {
            "id": "DOID:13137",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13137",
            "name": "progressive muscular atrophy of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Werdnig-Hoffmann disease",
            "description": "Proximal spinal muscular atrophy type 1 (SMA1) is a severe infantile form of proximal spinal muscular atrophy (see this term) characterized by severe and progressive muscle weakness and hypotonia resulting from the degeneration and loss of the lower motor neurons in the spinal cord and the brain stem nuclei."
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "SMA type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "SMA-I",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "survival motor neuron spinal muscular atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "spinal muscular atrophies of childhood",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Sma, infantile acute form",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "progressive muscular atrophy of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "infantile spinal muscular atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "severe infantile spinal muscular atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "spinal muscular atrophy, type I; SMA1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Werdnig-Hoffman disease",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Werdnig-Hoffmann disease",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "proximal spinal muscular atrophy, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "SMA type I",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "SMA1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Werdnig Hoffmann disease",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "Sma 1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "HMN (hereditary motor neuropathy) proximal type I",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "muscular atrophy, infantile",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "proximal spinal muscular atrophy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "infantile muscular atrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "spinal muscular atrophy, type I",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "hereditary motor neuropathy proximal type I",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "spinal muscular atrophy, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009669",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009669",
            "name": "spinal muscular atrophy 1",
            "description": ""
        },
        {
            "id": "MIM:253300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/253300",
            "name": "Spinal muscular atrophy 1",
            "description": "Spinal muscular atrophy 1"
        }
    ]
}