{
    "disease_id": "DOID:0080562", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "DPAGT1-CDG"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "carbohydrate deficient glycoprotein syndrome type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDG-Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "congenital disorder of glycosylation, type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDG 1J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "congenital disorder of glycosylation, type Ij; CDG1J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "DPAGT1-CDG (CDG-Ij)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDG syndrome type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "congenital disorder of glycosylation type Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDG Ij"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "dolichyl-phosphate N-acetylgalactosamine phosphotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDGIj"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "congenital disorder of glycosylation type 1j"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011964", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011964", 
            "name": "CDG1J"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080562", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080562", 
            "name": "Congenital disorder of glycosylation 1j"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080562", 
        "description": "A congenital disorder of glycosylation I that is characterized by hypotonia, intractable seizures, developmental delay, microcephaly and severe fetal hypokinesia and has_material_basis_in homozygous or compound heterozygous mutation in the DPAGT1 gene, which encodes UDP-GlcNAc:dolichyl-phosphate N-acetylglucosamine phosphotransferase, on chromosome 11q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080562", 
        "name": "congenital disorder of glycosylation Ij"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080562#disease-associations", 
            "id": "0080562", 
            "database": "Alliance of Genome Resources"
        }
    ]
}