{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "carnitine palmitoyl transferase 1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "disorder of carnitine cycle and carnitine transport caused by mutation in CPT1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "L-CPTI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "hepatic carnitine palmitoyl transferase I deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "CPT deficiency, hepatic, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "L-CPT 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "Carnitine palmitoyltransferase 1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "carnitine palmitoyl transferase IA deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "CPT I deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "Carnitine palmitoyl transferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "L-CPT1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "CPT1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "hepatic carnitine palmitoyl transferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "CPT 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "Carnitine Palmitoyltransferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "hepatic CPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "CPT1A disorder of carnitine cycle and carnitine transport"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009705", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009705", 
            "name": "hepatic CPT deficiency type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "CPT I deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "CPT1A deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "L-CPT1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "carnitine palmitoyl transferase 1A deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "carnitine palmitoyl transferase IA deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "hepatic CPT deficiency type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "hepatic carnitine palmitoyl transferase 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090129", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090129", 
            "name": "hepatic carnitine palmitoyl transferase I deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/255120", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:255120", 
            "name": "Carnitine palmitoyltransferase 1A deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090129", 
        "description": "A lipid metabolism disorder that is characterized by impaired mitochondrial oxidation of long chain fatty acids in the liver and kidneys resulting in episodes of illness- or fasting-induced hypoketotic hypoglycemia, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the carnitine palmitoyltransferase 1A gene (CPT1A) on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090129", 
        "name": "carnitine palmitoyltransferase I deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/255120", 
            "id": "255120", 
            "database": "MIM"
        }
    ]
}