{
    "disease_id": "DOID:0080053", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "pseudohypoparathyroidism type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "AHO"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "Albright hereditary osteodystrophy with multiple hormone resistance"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "Albright hereditary osteodystrophy-PHP syndrome Ia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "Albright hereditary osteodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "PHP 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "PHP1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "AHO-PHP syndrome Ia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "pseudohypoparathyroidism, type IA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "pseudohypoparathyroidism, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007078", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007078", 
            "name": "pseudohypoparathyroidism, type IA; PHP1A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080053", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080053", 
            "name": "Albright hereditary osteodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080053", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080053", 
            "name": "pseudohypoparathyroidism type 1a"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080053", 
        "description": "An pseudohypoparathyroidism that has_material_basis_in lack of responsiveness to parathyroid  hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080053", 
        "name": "Albright's hereditary osteodystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080053#disease-associations", 
            "id": "0080053", 
            "database": "Alliance of Genome Resources"
        }
    ]
}