{
    "disease_id": "DOID:0112186",
    "recommended_name": {
        "id": "DOID:0112186",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112186",
        "name": "thyroid dyshormonogenesis 2A",
        "description": "A familial thyroid dyshormonogenesis that has_material_basis_in homozygous or compound heterozygous mutation in TPO on chromosome 2p25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0112186",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112186",
            "name": "TDH2A",
            "description": ""
        },
        {
            "id": "DOID:0112186",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112186",
            "name": "genetic defect in thyroid hormonogenesis 2A",
            "description": ""
        },
        {
            "id": "DOID:0112186",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112186",
            "name": "iodide peroxidase deficiency",
            "description": ""
        },
        {
            "id": "DOID:0112186",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112186",
            "name": "thyroid peroxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "thyroid dyshormonogenesis 2A",
            "description": "Thyroid peroxidase system defect due to presumed mutation(s) in the TPO gene, resulting in decreased activity of thyroid peroxidase."
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "TDH2A",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "TPO familial thyroid dyshormonogenesis",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "familial thyroid dyshormonogenesis caused by mutation in TPO",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "hypothyroidism, congenital, due to dyshormonogenesis, 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "thyroid dyshormonogenesis 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "thyroid dyshormonogenesis type 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "thyroid hormonogenesis, genetic defect in, 2A",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "iodide peroxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010133",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010133",
            "name": "thyroid peroxidase deficiency",
            "description": ""
        },
        {
            "id": "MIM:274500",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/274500",
            "name": "Thyroid dyshormonogenesis 2A",
            "description": "Thyroid dyshormonogenesis 2A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112186"
    ],
    "unlinked_id_list": []
}