{
    "disease_id": "DOID:332", 
    "crossref_internal": {
        "protein": [
            "P00441-1"
        ]
    }, 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis type 1", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1; ALS1", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis, autosomal dominant", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1, autosomal recessive", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1, familial", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis, familial", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "ALS1", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "FALS", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis, sporadic", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis 1, autosomal dominant", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007103", 
            "resource": "MONDO", 
            "description": "", 
            "name": "amyotrophic lateral sclerosis, sporadic, included", 
            "id": "MONDO:0007103"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "ALS", 
            "id": "DOID:332"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "Lou Gehrig's disease", 
            "id": "DOID:332"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:332", 
            "resource": "Disease Ontology", 
            "description": "", 
            "name": "motor neuron disease, bulbar", 
            "id": "DOID:332"
        }, 
        {
            "url": "https://www.omim.org/entry/105400", 
            "resource": "MIM", 
            "description": "", 
            "name": "Amyotrophic lateral sclerosis 1", 
            "id": "MIM:105400"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:332", 
        "resource": "Disease Ontology", 
        "description": "A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.", 
        "name": "amyotrophic lateral sclerosis", 
        "id": "DOID:332"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/105400", 
            "id": "105400", 
            "database": "MIM"
        }
    ]
}