{
    "disease_id": "DOID:0070268", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "TMEM199-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "congenital disorder of glycosylation, type IIp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "congenital disorder of glycosylation, type IIp; CDG2P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "CDG IIp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "CDG syndrome type IIp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "congenital disorder of glycosylation type 2p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "CDG2P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "carbohydrate deficient glycoprotein syndrome type IIp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014790", 
            "name": "CDG-IIp"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "CDG IIp"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "CDG syndrome type IIp"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "CDG2P"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "CDGIIdp"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "Congenital disorder of glycosylation type 2p"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "TMEM199-CDG"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070268", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070268", 
            "name": "Carbohydrate deficient glycoprotein syndrome type IIp"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070268", 
        "description": "A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of TMEM199 on chromosome 17q11.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070268", 
        "name": "congenital disorder of glycosylation type IIp"
    }, 
    "evidence": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014790", 
            "id": "0014790", 
            "database": "MONDO"
        }, 
        {
            "url": "https://www.omim.org/entry/616829", 
            "id": "616829", 
            "database": "MIM"
        }
    ]
}