{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013802", 
            "name": "infantile cerebellar-retinal degeneration; ICRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013802", 
            "name": "ICRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013802", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013802", 
            "name": "infantile cerebellar retinal degeneration"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050883", 
        "description": "A neurodegenerative disease that is characterized by onset between ages 2 and 6 months of truncal hypotonia, athetosis, seizures, and ophthalmologic abnormalities, particularly optic atrophy and retinal degeneration.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050883", 
        "name": "infantile cerebellar-retinal degeneration"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614559", 
            "id": "614559", 
            "database": "MIM"
        }
    ]
}