{
    "disease_id": "DOID:0060357", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "CMRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "chylomicron retention disease; CMRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "CRD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "Anderson disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009528", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009528", 
            "name": "lipid Transport defect of intestine"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060357", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060357", 
            "name": "Anderson disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060357", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060357", 
            "name": "CMRD"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060357", 
        "description": "A lipid metabolism disorder characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and the absence of chylomicrons and apolipoprotein B48 post-prandially. It has an autosomal recessive inheritance pattern and has_material_basis_in mutations in the SAR1B gene on chromosome 5q31.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060357", 
        "name": "chylomicron retention disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060357#disease-associations", 
            "id": "0060357", 
            "database": "Alliance of Genome Resources"
        }
    ]
}