{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "SCAR21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "spinocerebellar ataxia, autosomal recessive 21; SCAR21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "spinocerebellar ataxia, autosomal recessive 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "spinocerebellar ataxia, autosomal recessive 21, with hepatopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "autosomal recessive spinocerebellar ataxia 21 with hepatopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "autosomal recessive spinocerebellar ataxia type 21"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014744", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014744", 
            "name": "spinocerebellar ataxia, autosomal recessive type 21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111155", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111155", 
            "name": "acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111155", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111155", 
            "name": "SCAR21"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111155", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111155", 
            "name": "autosomal recessive spinocerebellar ataxia 21 with hepatopathy"
        }, 
        {
            "url": "https://www.omim.org/entry/616719", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616719", 
            "name": "Spinocerebellar ataxia, autosomal recessive, 21"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111155", 
        "description": "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.", 
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        "name": "autosomal recessive spinocerebellar ataxia 21"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616719", 
            "id": "616719", 
            "database": "MIM"
        }
    ]
}