{
    "disease_id": "DOID:0090142", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009058", 
            "name": "cystathioninuria (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009058", 
            "name": "cystathionase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009058", 
            "name": "gamma-cystathionase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009058", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009058", 
            "name": "Cystathione gamma-lyase deficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090142", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090142", 
            "name": "cystathionase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090142", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090142", 
            "name": "cystathione gamma-lyase deficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090142", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090142", 
            "name": "gamma-cystathionase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090142", 
        "description": "An amino acid metabolic disorder that is characterized by elevated plasma and urinary cystathionine levels that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding cystathionine gamma-lyase (CTH) on chromosome 1p31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090142", 
        "name": "cystathioninuria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090142#disease-associations", 
            "id": "0090142", 
            "database": "Alliance of Genome Resources"
        }
    ]
}