{
    "disease_id": "DOID:0111455",
    "recommended_name": {
        "id": "DOID:0111455",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111455",
        "name": "GRACILE syndrome",
        "description": "A mitochondrial disorder characterized by fetal growth restriction, aminoaciduria, cholestasis, iron overload, lactocidosis, and early death that has_material_basis_in homozygous or compound heterozygous mutation in the BCS1L gene on chromosome 2q35."
    },
    "synonyms": [
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "FLNMS",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "Fellman disease",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "Finnish lactic acidosis with hepatic hemosiderosis",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "Finnish lethal neonatal metabolic syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111455",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111455",
            "name": "growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "GRACILE syndrome",
            "description": "GRACILE syndrome is an inherited lethal mitochondrial disorder characterized by fetal growth restriction (GR), aminoaciduria (A), cholestasis (C), iron overload (I), lactacidosis (L), and early death (E)."
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Fellman disease",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "gracile syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "FLNMS",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Fellman syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Finnish lactic acidosis with hepatic hemosiderosis",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Finnish lethal neonatal metabolic syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011308",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011308",
            "name": "Growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis and early death",
            "description": ""
        },
        {
            "id": "MIM:603358",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/603358",
            "name": "GRACILE syndrome",
            "description": "GRACILE syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111455"
    ],
    "unlinked_id_list": []
}