{
    "disease_id": "DOID:0080222", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "pseudohypoparathyroidism type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "pseudohypoparathyroidism, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "pseudohypoparathyroidism, type IB; PHP1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "Php 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "PHP1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011301", 
            "name": "pseudohypoparathyroidism, type IB"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080222", 
        "description": "A pseudohypoparathyroidism characterized by isolated renal parathyroid hormone (PTH) resistance resulting in hypocalcemia, hyperphosphatemia and elevated PTH levels that has_material_basis_in mutations that alter the methylation pattern of GNAS on 20q13.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080222", 
        "name": "pseudohypoparathyroidism type IB"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080222#disease-associations", 
            "id": "0080222", 
            "database": "Alliance of Genome Resources"
        }
    ]
}