{
    "disease_id": "DOID:0080062", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "GRM1 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "GRM1 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "spinocerebellar ataxia, autosomal recessive 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "SCAR13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "spinocerebellar ataxia, autosomal recessive 13; SCAR13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome caused by mutation in GRM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRM1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "autosomal recessive spinocerebellar ataxia type 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013905", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013905", 
            "name": "spinocerebellar ataxia, autosomal recessive type 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080062", 
        "description": "An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080062", 
        "name": "autosomal recessive spinocerebellar ataxia 13"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080062#disease-associations", 
            "id": "0080062", 
            "database": "Alliance of Genome Resources"
        }
    ]
}