{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "hypothyroidism, congenital, due to dyshormonogenesis, 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "PDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "thyroid hormonogenesis, genetic defect in, 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "autosomal recessive sensorineural hearing impairment and goiter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "TDH2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "thyroid dyshormonogenesis 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "goiter-deafness syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "Pendred syndrome; PDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "deafness with goiter"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "congenital hypothyroidism due to dyshormonogenesis 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010134", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010134", 
            "name": "genetic defect in thyroid hormonogenesis 2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "TDH2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "deafness with goiter"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "genetic defect in thyroid hormonogenesis 2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "goiter-deafness syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "thyroid dyshormonogenesis 2B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060744", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060744", 
            "name": "congenital hypothyroidism due to dyshormonogenesis 2B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060744", 
        "description": "A syndrome characterized by bilateral prelingual sensorineural hearing loss and euthyroid goiter and that has_material_basis_in homozygous or compound heterozygous mutation in the SLC26A4 gene on chromosome 7q.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060744", 
        "name": "Pendred Syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/274600", 
            "id": "274600", 
            "database": "MIM"
        }
    ]
}