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