{
    "disease_id": "DOID:0060357",
    "recommended_name": {
        "id": "DOID:0060357",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060357",
        "name": "chylomicron retention disease",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060357",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060357",
            "name": "Anderson disease",
            "description": ""
        },
        {
            "id": "DOID:0060357",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060357",
            "name": "CMRD",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "chylomicron retention disease",
            "description": "Chylomicron retention disease (CRD) is a type of familial hypocholesterolemia characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and hepatic, neurologic and ophthalmologic complications."
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "Anderson disease",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "CMRD",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "CRD",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "chylomicron retention disease",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "hypobetalipoproteinemia with accumulation of apolipoprotein B-like Protein in intestinal cells",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells",
            "description": ""
        },
        {
            "id": "MONDO:0009528",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009528",
            "name": "lipid Transport defect of intestine",
            "description": ""
        },
        {
            "id": "MIM:246700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/246700",
            "name": "Chylomicron retention disease",
            "description": "Chylomicron retention disease"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060357"
    ],
    "unlinked_id_list": []
}