{
    "disease_id": "DOID:0111587", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "cerebellar ataxia-hypogonadism syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "luteinizing hormone releasing hormone, deficiency of with ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "cerebellar ataxia and hypogonadotropic hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "cerebellar ataxia - hypogonadism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "Gordon-Holmes syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "LHRH deficiency and ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "GDHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "luteinizing hormone-releasing hormone deficiency with ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "Gordon Holmes syndrome; GDHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008935", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008935", 
            "name": "luteinizing hormone-releasing hormone, deficiency of, with ataxia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111587", 
            "name": "CAHH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111587", 
            "name": "GDHS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111587", 
            "name": "LHRH deficiency and ataxia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111587", 
            "name": "cerebellar ataxia-hypogonadism syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111587", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111587", 
            "name": "luteinizing hormone-releasing hormone deficiency with ataxia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111587", 
        "description": "An inherited metabolic disorder characterized by progressive cognitive decline, dementia, hypogonadotropic hypogonadism, and variable movement disorders resulting from disordered ubiquitination that has_material_basis_in homozygous or compound heterozygous mutation in RNF216 on chromosome 7p22.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111587", 
        "name": "Gordon Holmes syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111587#disease-associations", 
            "id": "0111587", 
            "database": "Alliance of Genome Resources"
        }
    ]
}