{
    "disease_id": "DOID:0051013",
    "recommended_name": {
        "id": "DOID:0051013",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0051013",
        "name": "pseudohypoparathyroidism type 1C",
        "description": "A pseudohypoparathyroidism that has_material_basis_in a heterozygous mutation on the maternal allele of the GNAS gene on chromosome 20q13."
    },
    "synonyms": [
        {
            "id": "DOID:0051013",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0051013",
            "name": "PHP Ic",
            "description": ""
        },
        {
            "id": "MONDO:0012911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012911",
            "name": "pseudohypoparathyroidism type 1C",
            "description": "A rare type of pseudohypoparathyroidism (PHP) characterized by resistance to parathyroid hormone (PTH) and other hormones, which manifests with hypocalcemia, hyperphosphatemia and elevated PTH levels, a constellation of clinical features collectively termed Albright's hereditary osteodystrophy (AHO), but normal activity of the stimulatory protein G (Gs alpha)."
        },
        {
            "id": "MONDO:0012911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012911",
            "name": "pseudohypoparathyroidism Ic",
            "description": ""
        },
        {
            "id": "MONDO:0012911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012911",
            "name": "PHP1C",
            "description": ""
        },
        {
            "id": "MONDO:0012911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012911",
            "name": "pseudohypoparathyroidism, type IC",
            "description": ""
        },
        {
            "id": "MIM:612462",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612462",
            "name": "Pseudohypoparathyroidism 1C",
            "description": "Pseudohypoparathyroidism 1C"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0051013"
    ],
    "unlinked_id_list": []
}