{
    "disease_id": "DOID:14701",
    "recommended_name": {
        "id": "DOID:14701",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14701",
        "name": "propionic acidemia",
        "description": "An organic acidemia that involes a nonfunctional propionyl CoA carboxylase affecting conversion of aminio acids and fats into sugar for energy."
    },
    "synonyms": [
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "GLYCINEMIA, KETOTIC",
            "description": ""
        },
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "KETOTIC HYPERGLYCINEMIA",
            "description": ""
        },
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "ketotic II glycinemia",
            "description": ""
        },
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "ketotic glycinemia",
            "description": ""
        },
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "propionic aciduria",
            "description": ""
        },
        {
            "id": "DOID:14701",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14701",
            "name": "propionyl-CoA carboxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "propionic acidemia",
            "description": "Propionic acidemia (PA) is an organic aciduria caused by the deficient activity of the propionyl Coenzyme A carboxylase and is characterized by life threatening episodes of metabolic decompensation, neurological dysfunction and that may be complicated by cardiomyopathy."
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "propionic aciduria",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "prop",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "propionyl-CoA carboxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "ketotic hyperglycinemia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "propionic acidemia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "Glycinemia, ketotic",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "propionyl-Coa carboxylase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "GLYCINEMIA, ketotic",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "hyperglycinemia with ketoacidosis and leukopenia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "Propionicacidemia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "ketotic II glycinemia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "ketotic glycinemia",
            "description": ""
        },
        {
            "id": "MONDO:0011628",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011628",
            "name": "PCC deficiency",
            "description": ""
        },
        {
            "id": "MIM:606054",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/606054",
            "name": "Propionic acidemia type I",
            "description": "Propionic acidemia type I"
        }
    ]
}