{
    "disease_id": "DOID:0111713",
    "recommended_name": {
        "id": "DOID:0111713",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111713",
        "name": "Temple syndrome",
        "description": "A syndrome characterized by low birth weight, hypotonia and motor delay, feeding problems early in life, early puberty, and significantly reduced final height that has_material_basis_in heterozygous mutation in an impriniting region on chromosome 14q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0014541",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014541",
            "name": "motor developmental delay due to 14q32.2 paternally expressed gene defect",
            "description": "A cause of obesity that results from inheritance of two copies of chromosome 14 from the mother, and no copy of chromosome 14 from the father."
        },
        {
            "id": "MONDO:0014541",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014541",
            "name": "mUPD14 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014541",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014541",
            "name": "uniparental disomy, maternal, chromosome 14",
            "description": ""
        },
        {
            "id": "MONDO:0014541",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014541",
            "name": "maternal uniparental disomy chromosome 14 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014541",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014541",
            "name": "TEMPLE syndrome",
            "description": ""
        }
    ]
}