{
    "disease_id": "DOID:13137", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "SMA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "infantile muscular atrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "hereditary motor neuropathy proximal type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "Spinal muscular atrophy 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "progressive muscular atrophy of infancy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13137", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13137", 
            "name": "HMN (Hereditary motor Neuropathy) Proximal type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "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.", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Werdnig-Hoffmann disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Werdnig-Hoffman disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "spinal muscular atrophy, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "spinal muscular atrophy, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "proximal spinal muscular atrophy type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "HMN (hereditary motor neuropathy) proximal type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "SMA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "hereditary motor neuropathy proximal type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "infantile spinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "SMA type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "muscular atrophy, infantile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "SMA type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "spinal muscular atrophy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "severe infantile spinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "spinal muscular atrophies of childhood"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Sma 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "infantile muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Werdnig Hoffmann disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "proximal spinal muscular atrophy, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "SMA-I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "survival motor neuron spinal muscular atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "spinal muscular atrophy, type I; SMA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Werdnig-Hoffmann disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "Sma, infantile acute form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009669", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009669", 
            "name": "progressive muscular atrophy of infancy"
        }, 
        {
            "url": "https://www.omim.org/entry/253300", 
            "description": "Spinal muscular atrophy 1", 
            "resource": "MIM", 
            "id": "MIM:253300", 
            "name": "Spinal muscular atrophy 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13137", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:13137", 
        "name": "Werdnig-Hoffmann disease"
    }
}