{
    "disease_id": "DOID:0050781", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "NAT1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "N acetyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "Acetyl-CoA:arylamine n-acetyltransferase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "arylamine n-acetyltransferase 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "Ogden syndrome; OGDNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "N acetyltransferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "X-linked malformation and infantile lethality syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "OGDNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "N-terminal acetyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "N-alpha-acetyltransferase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010457", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010457", 
            "name": "premature aging appearance-developmental delay-cardiac arrhythmia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050781", 
            "name": "N-alpha-acetyltransferase"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050781", 
            "name": "N-terminal acetyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050781", 
            "name": "OGDNS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050781", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050781", 
            "name": "X-linked Malformation and Infantile Lethality Syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050781", 
        "description": "A syndrome characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia and has_material_basis_in X-linked recessive or X-linked dominant mutation in the NAA10 gene on chromosome Xq28.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050781", 
        "name": "Ogden syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050781#disease-associations", 
            "id": "0050781", 
            "database": "Alliance of Genome Resources"
        }
    ]
}