{
    "disease_id": "DOID:0060235", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "carnitine palmitoyl transferase II deficiency, myopathic form"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "CPTII, myopathic form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine Palmitoyltransferase 2 deficiency, myopathic, stress-induced"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "CARNITINE PALMITOYLTRANSFERASE II deficiency, myopathic, stress-induced"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine palmitoyl transferase II deficiency, adult-onset form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "CARNITINE PALMITOYLTRANSFERASE II deficiency, late-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine Palmitoyltransferase 2 deficiency, myopathic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "CPT 2 deficiency, myopathic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Cpt2 deficiency, late-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "CPT2, adult-onset form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine Palmitoyltransferase 2 deficiency, adult-onset"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine palmitoyl transferase deficiency type 2, adult-onset form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "CPT2, myopathic form"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009704", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009704", 
            "name": "Carnitine palmitoyl transferase deficiency type 2, myopathic form"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060235", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060235", 
            "name": "late-onset carnitine palmitoyltransferase II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060235", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060235", 
            "name": "infantile carnitine palmitoyltransferase II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060235", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060235", 
            "name": "CPT-II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060235", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060235", 
            "name": "lethal neonatal carnitine palmitoyltransferase II deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/255110", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:255110", 
            "name": "Carnitine palmitoyltransferase 2 deficiency, myopathic, stress-induced"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060235", 
        "description": "A lipid metabolism disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060235", 
        "name": "carnitine palmitoyltransferase II deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/255110", 
            "id": "255110", 
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        }, 
        {
            "url": "https://www.omim.org/entry/600649", 
            "id": "600649", 
            "database": "MIM"
        }, 
        {
            "url": "https://www.omim.org/entry/608836", 
            "id": "608836", 
            "database": "MIM"
        }
    ]
}