{
    "disease_id": "DOID:0080502", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "infantile GM1 gangliosidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "GLB deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "gangliosidosis, generalized GM1, type I, with Cardiac involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "gangliosidosis generalized GM1 type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "GM1-gangliosidosis, type I, with Cardiac involvement"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "GM1-gangliosidosis, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "Norman-Landing disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "Glb1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "gangliosidosis generalized GM1 infantile form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "Beta galactosidase deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "gangliosidosis, generalized GM1, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "GM1-gangliosidosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "Beta-galactosidase-1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009260", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009260", 
            "name": "gangliosidosis, generalized GM1, infantile form"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080502", 
        "description": "A GM1 gangliosidosis that is characterized by rapid psychomotor deterioration beginning within 6 months of birth, generalized central nervous system involvement, hepatosplenomegaly, facial dysmorphism, macular cherry-red spots, skeletal dysplasia, and early death.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080502", 
        "name": "GM1 gangliosidosis type 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080502#disease-associations", 
            "id": "0080502", 
            "database": "Alliance of Genome Resources"
        }
    ]
}