{
    "disease_id": "DOID:0111065", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "autosomal recessive distal spinal muscular atrophy 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "spinal muscular atrophy, Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "spinal muscular atrophy Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "motor neuropathy, distal, Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "DSMA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "hereditary motor neuropathy, Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 2; DSMA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "autosomal recessive distal spinal muscular atrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "MNDJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "distal hereditary motor neuropathy Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "dHMNJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "neuronopathy, distal hereditary motor, Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "distal hereditary motor neuropathy, Jerash type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "HMNJ"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "spinal muscular atrophy, distal, autosomal recessive, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011585", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011585", 
            "name": "neuropathy, distal hereditary motor, Jerash type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111065", 
            "name": "DSMA2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111065", 
            "name": "dHMNJ"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111065", 
            "name": "distal hereditary motor neuropathy Jerash type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111065", 
            "name": "spinal muscular atrophy Jerash type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111065", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111065", 
            "name": "autosomal recessive distal spinal muscular atrophy 2"
        }, 
        {
            "url": "https://www.omim.org/entry/605726", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:605726", 
            "name": "Distal spinal muscular atrophy, autosomal recessive, 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111065", 
        "description": "A spinal muscular atrophy characterized by autosomal recessive inheritance of distal muscle weakness and muscle wasting primarily affecting the upper and lower limbswith onset typically in the first decade of life that has_material_basis_in homozygous mutation in the SIGMAR1 gene on chromosome 9p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111065", 
        "name": "distal spinal muscular atrophy 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/605726", 
            "id": "605726", 
            "database": "MIM"
        }
    ]
}