{
    "disease_id": "DOID:332", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1; ALS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1, autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "ALS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "FALS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis, sporadic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis 1, autosomal dominant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007103", 
            "name": "amyotrophic lateral sclerosis, sporadic, included"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:332", 
            "name": "ALS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:332", 
            "name": "Lou Gehrig's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:332", 
            "name": "motor neuron disease, bulbar"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:332", 
        "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.", 
        "resource": "Disease Ontology", 
        "id": "DOID:332", 
        "name": "amyotrophic lateral sclerosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/332#disease-associations", 
            "id": "332", 
            "database": "Alliance of Genome Resources"
        }
    ]
}