{
    "disease_id": "DOID:0090123", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012084", 
            "name": "DDC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012084", 
            "name": "Dopa decarboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012084", 
            "name": "AADC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012084", 
            "name": "aromatic L-amino-acid decarboxylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012084", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012084", 
            "name": "aromatic amino acid decarboxylase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090123", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090123", 
            "name": "AADC deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090123", 
        "description": "An inherited metabolic disorder that is characterized by reduced production of serotonin and dopamine resulting in hypotonia, hypokinesia, ptosis oculogyric crises, and signs of autonomic dysfunction, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the dopa decarboxylase gene (DDC) on chromosome 7p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090123", 
        "name": "aromatic L-amino acid decarboxylase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090123#disease-associations", 
            "id": "0090123", 
            "database": "Alliance of Genome Resources"
        }
    ]
}