{
    "disease_id": "DOID:0111037", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011698", 
            "name": "hypermethioninemia due to GNMT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011698", 
            "name": "GNMT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011698", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011698", 
            "name": "hypermethioninemia due to glycine N-methyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111037", 
            "name": "GNMT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111037", 
            "name": "hypermethioninemia due to GNMT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111037", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111037", 
            "name": "hypermethioninemia due to glycine N-methyltransferase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111037", 
        "description": "A hypermethioninemia characterized by autosomal recessive inheritance of persistent isolated hypermethioninemia without cystathionine beta-synthase deficiency, tyrosinemia type I, or liver disease that has material_basis_in homozygous or compound heterozygous mutation in the GNMT gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111037", 
        "name": "glycine N-methyltransferase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111037#disease-associations", 
            "id": "0111037", 
            "database": "Alliance of Genome Resources"
        }
    ]
}