{
    "disease_id": "DOID:0111535",
    "recommended_name": {
        "id": "DOID:0111535",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111535",
        "name": "progressive osseous heteroplasia",
        "description": "A syndrome characterized by infantile onset of dermal ossification followed by progressive bone formation in skeletal muscle and deep fascia that has_material_basis_in heterozygous loss of function mutation in the Gs-alpha isoform of GNAS on chromosome 20q13.32."
    },
    "synonyms": [
        {
            "id": "DOID:0111535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111535",
            "name": "POH",
            "description": ""
        },
        {
            "id": "DOID:0111535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111535",
            "name": "ectopic ossification familial type",
            "description": ""
        },
        {
            "id": "DOID:0111535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111535",
            "name": "familial ectopic ossification",
            "description": ""
        },
        {
            "id": "DOID:0111535",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111535",
            "name": "osteoma cutis",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "progressive osseous heteroplasia",
            "description": "gene (20q13.2-q13.3), coding for guanine nucleotide-binding proteins. POH can, however, be distinguished clinically by the deep and progressive nature of the heterotopic bone formation."
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "osteoma cutis",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "poh",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "osseous heteroplasia, progressive",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "osseous heteroplasia, progressive; poh",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "familial ectopic ossification",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "ectopic ossification familial type",
            "description": ""
        },
        {
            "id": "MONDO:0008153",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008153",
            "name": "ectopic ossification, familial",
            "description": ""
        },
        {
            "id": "MIM:166350",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/166350",
            "name": "Progressive osseous heteroplasia",
            "description": "Progressive osseous heteroplasia"
        }
    ]
}