{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "autosomal recessive lower motor neuron disease with childhood onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "autosomal recessive distal spinal muscular atrophy type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "dSMA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 4; DSMA4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012608", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012608", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, type 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111213", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111213", 
            "name": "DSMA4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111213", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111213", 
            "name": "autosomal recessive lower motor neuron disease with childhood onset"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111213", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111213", 
            "name": "autosomal recessive distal spinal muscular atrophy type 4"
        }, 
        {
            "url": "https://www.omim.org/entry/611067", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:611067", 
            "name": "Distal spinal muscular atrophy, autosomal recessive, 4"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111213", 
        "description": "An autosomal recessive distal hereditary motor neuronopathy characterized by onset in early childhood of rapidly progressing proximal muscle weakness with an early involvement of foot and hand muscles that has_material_basis_in homozygous or compound heterozygous mutation in PLEKHG5 on 1p36.31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111213", 
        "name": "distal spinal muscular atrophy type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/611067", 
            "id": "611067", 
            "database": "MIM"
        }
    ]
}