{
    "disease_id": "DOID:13372", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:13372", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13372", 
            "name": "AAT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "Alpha-1-antitrypsin deficiency is a hereditary disease that develops in adulthood and is characterized by chronic liver disorders (cirrhosis), respiratory disorders (emphysema), and rarely panniculitis.", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "alpha 1-antitrypsin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "A1AT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "deficiency in Alpa-1-proteinase inhibitor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "A1AD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "A-1ATD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "alpha-1-antitrypsin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "A1ATD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "Alpha 1 antitrypsin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "AATD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "AAT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "Alpha-1 antitrypsin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013282", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013282", 
            "name": "ALPHA-1-antitrypsin deficiency; A1ATD"
        }, 
        {
            "url": "https://www.omim.org/entry/613490", 
            "description": "Alpha-1-antitrypsin deficiency", 
            "resource": "MIM", 
            "id": "MIM:613490", 
            "name": "Alpha-1-antitrypsin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13372", 
        "description": "A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells.", 
        "resource": "Disease Ontology", 
        "id": "DOID:13372", 
        "name": "alpha 1-antitrypsin deficiency"
    }
}