{
    "disease_id": "DOID:0080567", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "ALG11-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "congenital disorder of glycosylation type 1p"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "congenital disorder of glycosylation, type Ip; CDG1P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "CDG-Ip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "carbohydrate deficient glycoprotein syndrome type Ip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "ALG11-CDG (CDG-Ip)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "CDG1P"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "CDG syndrome type Ip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "congenital disorder of glycosylation type Ip"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013349", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013349", 
            "name": "congenital disorder of glycosylation, type Ip"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080567", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080567", 
            "name": "congenital disorder of glycosylation 1p"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080567", 
        "description": "A congenital disorder of glycosylation I that is characterized by facial dysmorphism (microcephaly, high forehead, low posterior hairline, strabismus), hypotonia, failure to thrive, intractable seizures, developmental delay, persistent vomiting and gastric bleeding and has_material_basis_in homozygous or compound heterozygous mutation in the ALG11 gene on chromosome 13q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080567", 
        "name": "congenital disorder of glycosylation Ip"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080567#disease-associations", 
            "id": "0080567", 
            "database": "Alliance of Genome Resources"
        }
    ]
}