{
    "disease_id": "DOID:0060196", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "ALS 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "dHMN with upper motor neuron signs"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "SETX amyotrophic lateral sclerosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "neuronopathy, distal hereditary motor, with pyramidal features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "amyotrophic lateral sclerosis caused by mutation in SETX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "distal hereditary motor neuropathy with pyramidal features"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "amyotrophic lateral sclerosis 4, juvenile; ALS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "ALS4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "amyotrophic lateral sclerosis 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "amyotrophic lateral sclerosis 4, juvenile"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011223", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011223", 
            "name": "distal hereditary motor neuropathy with upper motor neuron signs"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "ALS 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "distal hereditary motor neuropathy with pyramidal features"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "amyotrophic lateral sclerosis 4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "amyotrophic lateral sclerosis 4, juvenile"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "dHMN with upper motor neuron signs"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060196", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060196", 
            "name": "distal hereditary motor neuropathy with upper motor neuron signs"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060196", 
        "description": "An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060196", 
        "name": "amyotrophic lateral sclerosis type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060196#disease-associations", 
            "id": "0060196", 
            "database": "Alliance of Genome Resources"
        }
    ]
}