{
    "disease_id": "DOID:0112307",
    "recommended_name": {
        "id": "DOID:0112307",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112307",
        "name": "sarcosinemia",
        "description": "An amino acid metabolic disorder characterized by increased concentrations of sarcosine in plasma and urine that has_material_basis_in homozygous or compound heterozygous mutation in the SARDH gene on chromosome 9q34.2."
    },
    "synonyms": [
        {
            "id": "DOID:0112307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112307",
            "name": "SARCOS",
            "description": ""
        },
        {
            "id": "DOID:0112307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112307",
            "name": "SARD deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112307",
            "name": "SARDH deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112307",
            "name": "demethylation defect of N-methylglycine",
            "description": ""
        },
        {
            "id": "DOID:0112307",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112307",
            "name": "sarcosine dehydrogenase complex deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "sarcosinemia",
            "description": "Sarcosinemia is a metabolic disorder characterized by an increased concentration of sarcosine in plasma and urine due to sarcosine dehydrogenase deficiency."
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "sarcosinemia",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "SARCOS",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "SARD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "SARDH deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "hypersarcosinemia",
            "description": ""
        },
        {
            "id": "MONDO:0010008",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010008",
            "name": "sarcosine dehydrogenase complex deficiency",
            "description": ""
        },
        {
            "id": "MIM:268900",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/268900",
            "name": "Sarcosinemia",
            "description": "Sarcosinemia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112307"
    ],
    "unlinked_id_list": []
}